Pharmacovigilance Hiring at Accenture

Pharmacovigilance Hiring at Accenture

Pharmacovigilance Hiring at Accenture

Key Points for Job Seekers

DetailsInformation
PositionPharmacovigilance Services Associate
CompanyAccenture
Experience Required0 – 1 year
Salary Range₹4,00,000 – ₹7,00,000 per year
LocationBangalore
Job TypeFull-Time
Educational QualificationsBachelor of Pharmacy (B.Pharm)
Job HighlightsWork-Life Balance, Time Management, Flexibility, Problem Solving
ResponsibilitiesMailbox Management, Case Processing, MedDRA Coding, Timely ICSR Submissions
Skills RequiredAttention to Detail, Team Collaboration, Adaptability, Technical Proficiency

Step Into Pharmacovigilance with Accenture

Accenture, a global leader in professional services, is offering an exciting opportunity for aspiring professionals to launch their careers in pharmacovigilance. As a Pharmacovigilance Services Associate, you’ll join a world-class organization that combines cutting-edge technology and human ingenuity to create meaningful change. If you’re a recent graduate looking to kick-start your career, this role offers an excellent entry point into the life sciences industry. Pharmacovigilance Hiring at Accenture


About Accenture

Accenture is renowned for its innovative approach to solving complex challenges. Operating in over 120 countries, the company provides services across Strategy & Consulting, Technology, Operations, and Accenture Song. With a workforce of over 699,000 professionals, Accenture’s Life Sciences R&D vertical focuses on supporting biopharma companies with essential services like clinical trials, regulatory processes, pharmacovigilance, and patient support. Pharmacovigilance Hiring at Accenture

Pharmacovigilance Hiring at Accenture
Pharmacovigilance Hiring at Accenture

Why Choose This Role?

As a Pharmacovigilance Services Associate, you’ll be part of a dynamic environment where innovation meets purpose. Here’s why this role stands out:

  • Entry-Level Opportunity: No prior experience required; suitable for recent graduates.
  • Competitive Salary: Earn between ₹4-7 LPA.
  • Professional Growth: Gain hands-on experience in pharmacovigilance, a critical field in healthcare.
  • Global Exposure: Be part of a company with a strong international presence.

Your Role and Responsibilities

In this role, you will play a crucial part in ensuring the safety and efficacy of pharmaceuticals. Your primary tasks will include:

  • Managing the Affiliate Mailbox: Reconciling reports and ensuring accurate documentation.
  • Follow-Up Activities: Handling both serious and non-serious case follow-ups in written form.
  • Case Processing: Creating and managing case entries, including MedDRA coding and data entry.
  • ICSR Submission: Ensuring timely submission of Individual Case Safety Reports as per client and regulatory guidelines.
  • Team Collaboration: Working closely with team members and supervisors while following task instructions.
  • Shift Work: Adapting to rotational shifts as required by project needs.
    Pharmacovigilance Hiring at Accenture

What You’ll Need to Succeed

Accenture is looking for candidates who exhibit the following skills and attributes:

  1. Attention to Detail: Ensure precision in case processing and data entry.
  2. Team Collaboration: Work effectively within a team to achieve shared goals.
  3. Adaptability: Thrive under supervision and handle routine tasks with ease.
  4. Flexibility: Be open to working in rotational shifts to meet project requirements.
  5. Technical Proficiency: Familiarity with MedDRA coding, data entry, and safety databases is a plus.
    Pharmacovigilance Hiring at Accenture
Pharmacovigilance Hiring at Accenture
Pharmacovigilance Hiring at Accenture

Qualifications and Experience

To be eligible for this role, you need:

  • A Bachelor’s Degree in Pharmacy (B.Pharm).
  • 0–1 year of experience in pharmacovigilance or a related field (freshers are welcome to apply).
  • Proficiency in English, both written and verbal.
    Pharmacovigilance Hiring at Accenture

A Glimpse into Your Future with Accenture

This role offers more than just a paycheck. It’s an opportunity to build a career in pharmacovigilance, one of the most vital fields in life sciences. At Accenture, you’ll benefit from:

  • Work-Life Balance: Enjoy a structured schedule and a supportive work environment.
  • Professional Development: Gain exposure to global projects and cutting-edge tools.
  • Collaborative Culture: Work with a team that values innovation, collaboration, and excellence.
    Pharmacovigilance Hiring at Accenture

How to Apply

Ready to embark on this exciting journey? Submit your application online today and take the first step toward a rewarding career with Accenture. Don’t miss this opportunity to work with one of the world’s leading professional services firms. Apply now and make an impact in the field of pharmacovigilance! Pharmacovigilance Hiring at Accenture

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Pharmacovigilance Hiring at Accenture
Pharmacovigilance Hiring at Accenture

Regulatory Affairs Officer at Cliantha Research

Regulatory Affairs Officer at Cliantha Research

Regulatory Affairs Officer at Cliantha Research


Job Overview

Job TitleRegulatory Affairs Officer
CompanyCliantha Research
LocationAhmedabad, India
Experience Required0 – 2 years in Regulatory Affairs
Annual Salary₹1.75 – ₹3 Lakhs
Education RequiredBachelor’s Degree in Pharmacy (B.Pharm)
Application ModeOnline Application
Additional NotesOnly candidates with B.Pharm qualifications; M.Pharm or higher will not be considered.

Regulatory Affairs Officer at Cliantha Research


About Cliantha Research

Cliantha Research is a leading clinical research organization (CRO) focused on advancing scientific research for the pharmaceutical and healthcare sectors. With a commitment to maintaining the highest regulatory standards, Cliantha offers robust solutions across drug development, regulatory compliance, and quality management. As a Regulatory Affairs Officer at Cliantha, you will play a key role in ensuring that all documentation and applications meet national regulatory standards. Regulatory Affairs Officer at Cliantha Research


Job Highlights

  • Work/Life Balance: Emphasis on maintaining a balance between work responsibilities and personal life.
  • Time Management: Encouragement to meet regulatory deadlines while managing priorities.
  • Flexibility: Opportunity to work across a variety of regulatory tasks.
  • Problem-Solving: Environment supportive of innovative approaches to regulatory challenges.
    Regulatory Affairs Officer at Cliantha Research

Key Responsibilities

In this role, the Regulatory Affairs Officer will be responsible for the following:

  • Documentation Review and Finalization: Work with managers to review and finalize all documentation required by the Drugs Controller General of India (DCGI).
  • Submission Management: Handle the submission of BE-NOC (Bioequivalence No Objection Certificate) and T-license applications, ensuring strict adherence to DCGI guidelines.
  • Query Handling: Address any queries related to submitted applications, collaborating with team members to ensure accurate responses.
  • Regulatory Tracking: Monitor the progress of regulatory submissions and approvals, maintaining updates on a centralized common drive accessible across Cliantha locations.
  • Record Maintenance: Keep an updated regulatory tracking sheet for all submitted applications, approvals, and notifications.
    Regulatory Affairs Officer at Cliantha Research
Regulatory Affairs Officer at Cliantha Research
Regulatory Affairs Officer at Cliantha Research

Required Qualifications

  • Education: A Bachelor’s degree in Pharmacy (B.Pharm) is mandatory.
  • Knowledge: Basic understanding of regulatory processes within the pharmaceutical industry, especially concerning documentation and compliance.
  • Note: Candidates with M.Pharm or higher qualifications are not eligible for this role.

Key Skills and Attributes

To succeed in the role, ideal candidates should possess:

  1. Attention to Detail: High accuracy in managing documentation and compliance requirements.
  2. Organizational Skills: Capability to manage multiple submissions efficiently, track approvals, and ensure timeliness.
  3. Communication: Strong written and verbal communication skills for collaborating with managers and regulatory bodies.
  4. Proactivity: Ability to anticipate and address regulatory needs and deadlines.
  5. Team Collaboration: Effective teamwork skills for coordination with multiple departments and ensuring regulatory deadlines are met.

Benefits of Working at Cliantha Research

  • Professional Growth: Hands-on experience in regulatory affairs within a leading CRO.
  • Collaborative Environment: Work with a skilled team dedicated to maintaining high standards in regulatory compliance.
  • Learning Opportunities: Exposure to comprehensive training and development in regulatory processes.
    Regulatory Affairs Officer at Cliantha Research

How to Apply

Interested candidates who meet the qualifications are encouraged to apply online. Please ensure that you meet the criteria of having a B.Pharm degree and a foundational understanding of regulatory documentation in the pharmaceutical sector.

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Regulatory Affairs Officer at Cliantha Research
Regulatory Affairs Officer at Cliantha Research

FAQs

1. What does the Regulatory Affairs Officer role entail?

  • The position involves coordinating and submitting regulatory documentation in compliance with DCGI guidelines, managing the application process for BE-NOC and T-license, and maintaining accurate records.

2. What is the salary range for this position?

  • The annual salary for this role ranges from ₹1.75 to ₹3 Lakhs.

3. Why should I consider a career with Cliantha Research?

  • Cliantha Research offers a supportive work culture, opportunities for career growth, and the chance to work with a dedicated team in a leading clinical research organization.

This position at Cliantha Research presents an excellent opportunity for professionals starting their careers in regulatory affairs to gain valuable industry experience in a collaborative and detail-oriented environment. Apply now to join a team committed to regulatory excellence and contribute to impactful healthcare advancements.

Regulatory Affairs Officer at Cliantha Research
Regulatory Affairs Officer at Cliantha Research

Junior Assistant Production at Serigen

Junior Assistant Production at Serigen

Junior Assistant Production at Serigen

Company: Serigen
Location: Electronic Co-operative Industrial Estate, Parvati Paytha, Pune
Position: Junior Assistant Production
Experience Required: 0 – 2 years (Fresh graduates are welcome)
Qualification: Bachelor’s degree in Chemistry, Biochemistry, or Biotechnology
Job Type: Full-time, Work from Office
Application Mode: Online Application


Job Highlights

FeatureDetails
Work/Life BalanceSupportive and flexible environment
Time ManagementEmphasis on effective time utilization
FlexibilityAdaptability to production demands
Problem SolvingEncouraged to find solutions in production

About Serigen

Serigen is a forward-thinking company dedicated to the advancement of tissue generation products and biomedical devices. Known for its cutting-edge work in wound care and tissue regeneration, Serigen is on a mission to lead the field globally by prioritizing innovation and maintaining the highest standards of product quality. This role offers a unique opportunity to contribute to Serigen’s vision and play a part in transforming patient care through high-quality biomedical solutions. Junior Assistant Production at Serigen


Job Details

Job Title: Junior Assistant Production
Location: Electronic Co-operative Industrial Estate, Parvati Paytha, Pune
Employment Type: Full-time (On-site)


Key Responsibilities

As a Junior Assistant Production, you will be involved in various activities to support the efficient manufacturing of wound care products. Responsibilities include:

  • Production Tasks: Execute routine production processes, adhering to quality and safety standards.
  • Equipment Calibration: Perform calibration and maintenance of production equipment to ensure compliance and accuracy.
  • Data and Compliance: Maintain regular data entry, adhering to ISO 13485 standards for production documentation.
  • Additional Tasks: Carry out other production-related tasks as assigned by the reporting officer.
    Junior Assistant Production at Serigen
Junior Assistant Production at Serigen
Junior Assistant Production at Serigen

Candidate Profile

Education Requirements:

  • Bachelor’s degree in Chemistry, Biochemistry, or Biotechnology.

Experience Requirements:

  • 0 to 2 years of relevant experience in a production setting. Fresh graduates are encouraged to apply.

Preferred Skills:

  • Familiarity with laboratory instruments, such as centrifuges and pH meters, is preferred.
  • Proficiency in time management, attention to detail, and adaptability.
  • Strong problem-solving skills to handle production challenges.
    Junior Assistant Production at Serigen
Junior Assistant Production at Serigen
Junior Assistant Production at Serigen

Why Join Serigen?

Working at Serigen provides an enriching experience in the field of biomedical innovation. As part of a dedicated team, you will contribute to groundbreaking products that impact patient lives positively.

  • Career Growth: Serigen offers opportunities for skill development and career advancement.
  • Innovative Environment: Be a part of a team that values creativity and innovation.
  • Supportive Work Culture: Serigen promotes work-life balance, flexibility, and encourages employees to bring forth solutions to enhance productivity. Junior Assistant Production at Serigen

How to Apply

Interested candidates can apply through either of the following methods:

  • Google Form: Complete the application form via Apply Here.
  • Email Submission: Send your updated CV to hr@serigenmed.com with the subject line “Application for Junior Assistant Production – Serigen.”

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Take your first step towards a rewarding career in the biomedical field. Join Serigen to make a difference in healthcare innovation!

Junior Assistant Production at Serigen
Junior Assistant Production at Serigen

Lab Report Coordinator Intern at ICON Plc

Lab Report Coordinator Intern at ICON Plc

Lab Report Coordinator Intern at ICON Plc

Position: Lab Report Coordinator Intern
Company: ICON Plc
Location: Bangalore, India
Experience Level: 0-1 year (Freshers welcome)
Eligibility: Bachelor’s degree in Medical Laboratory Technology (MLT) or related field (B.Sc. MLT)
Job Type: Verified, Online Application


Company Overview

ICON Plc is a global leader in providing development and commercialization services to the pharmaceutical, biotechnology, and medical device industries. With a strong focus on advancing healthcare through innovative research and development (R&D) solutions, ICON is renowned for its excellence in lab results entry, data analysis, and process improvement. ICON’s inclusive work culture and commitment to employees, clients, and performance make it an ideal employer for those looking to launch or grow their career in the pharmaceutical and life sciences sectors. Lab Report Coordinator Intern at ICON Plc

Job Highlights

  • Work/Life Balance: Supportive work environment with flexible hours.
  • Time Management: Encourages efficient management of tasks and responsibilities.
  • Flexibility: Hands-on experience in lab report coordination.
  • Problem-Solving: Opportunities to develop problem-solving skills in a collaborative setting.
    Lab Report Coordinator Intern at ICON Plc

Key Responsibilities

As a Lab Report Coordinator Intern, you will play an essential role in ensuring accuracy and integrity in lab report data entry. You will be responsible for entering lab results and verifying patient demographics within ICON’s iRIS system, adhering to company guidelines. Key responsibilities include: Lab Report Coordinator Intern at ICON Plc

Lab Report Coordinator Intern at ICON Plc
Lab Report Coordinator Intern at ICON Plc
  1. Data Entry of Lab Results
  • Accurately enter lab results and reference ranges into the system following sponsor and departmental requirements.
  • Use reference guides for translating lab results and ensure all data entries meet required standards.
  1. Verification and Quality Control
  • Verify patient demographics, visit details, and other critical information to maintain accuracy.
  • Identify discrepancies in lab reports and resolve issues in collaboration with team members.
  1. Accession Updates and Query Responses
  • Update accessions by responding to site queries and entering calculated results as needed.
  • Ensure all entries align with ICON’s commitment to seamless, high-quality data management.
  1. Support Process Improvement Initiatives
  • Actively participate in ICON’s process improvement culture, contributing to effective data handling and coordination.
    Lab Report Coordinator Intern at ICON Plc

Qualifications and Skills Required

To qualify for the Lab Report Coordinator Intern position, candidates should meet the following criteria:

  • Education: A Bachelor’s degree in Medical Laboratory Technology (MLT) or a related field, such as B.Sc. MLT. Recent graduates (2024) with no academic backlogs are encouraged to apply.
  • Skills:
  • Communication: Strong verbal and written communication skills for accurate documentation and collaboration.
  • Attention to Detail: High accuracy in data entry, essential for managing lab reports.
  • Technical Proficiency: Familiarity with laboratory information systems (LIS) and Microsoft Office Suite.
  • Team Collaboration: Ability to work effectively within a team-oriented environment.
  • Lab Knowledge: Understanding of laboratory procedures and data entry systems.
  • Problem-Solving: Ability to identify and resolve discrepancies in lab data, ensuring accuracy and compliance.
    Lab Report Coordinator Intern at ICON Plc
Lab Report Coordinator Intern at ICON Plc
Lab Report Coordinator Intern at ICON Plc

Application Process

How to Apply: Interested candidates can apply online by submitting their application through ICON’s official careers portal.

To make the most of the application process, ensure you:

  • Update Your CV: Highlight relevant skills, academic projects, or any lab-related experience.
  • Prepare for Data Entry Tests: Familiarize yourself with lab data entry practices and LIS.
  • Showcase Your Skills: Emphasize your attention to detail, proficiency in laboratory software, and experience in team collaboration.
    Lab Report Coordinator Intern at ICON Plc

Interview Preparation Tips

  1. Understand the Role: Review the job responsibilities to understand the specific duties and challenges of lab report coordination.
  2. Highlight Relevant Skills: Be prepared to discuss your knowledge of laboratory information systems and your experience (if any) in data entry tasks.
  3. Demonstrate Problem-Solving Abilities: Emphasize any relevant experience or coursework that demonstrates your ability to identify and correct errors or discrepancies.
  4. Showcase Communication Skills: Good communication is essential, so practice describing your previous projects or coursework clearly.

Why Join ICON Plc?

ICON Plc offers a supportive, inclusive work culture that promotes growth, learning, and career advancement. Employees at ICON benefit from:

  • Mentorship and Learning Opportunities: Gain experience with advanced lab data entry techniques and systems.
  • Career Development: ICON’s commitment to innovation and quality provides an excellent environment for building a career in bioanalytics and clinical research.
  • Team-Oriented Culture: Work within a collaborative and professional team that values problem-solving and integrity.
    Lab Report Coordinator Intern at ICON Plc

Additional Job Highlights

Key FeatureDetails
PositionLab Report Coordinator Intern
LocationBangalore, India
Experience Required0-1 year
Skills EmphasizedData accuracy, communication, problem-solving
Application ModeOnline Application
Education RequiredB.Sc. MLT or related field
Lab Report Coordinator Intern at ICON Plc
Lab Report Coordinator Intern at ICON Plc

Takeaway: The Lab Report Coordinator Intern position at ICON Plc is ideal for recent MLT graduates who are eager to gain experience in lab report coordination, data entry, and laboratory information systems. This role offers a unique opportunity to begin a career in clinical research and pharmaceutical development with a respected global leader in healthcare solutions.

Analyst Bioanalytical Research at Veeda Clinical Research

Analyst Bioanalytical Research at Veeda Clinical Research

Analyst Bioanalytical Research at Veeda Clinical Research

Position: Analyst – Bioanalytical Research
Company: Veeda Clinical Research (Veeda CR)
Location: Ahmedabad, Gujarat
Experience Level: 0-3 years
Eligibility: Bachelor’s or Master’s degree in Life Sciences, Chemistry, Biotechnology, or a related field
Job Type: Verified, Walk-in Interview


Company Overview

Veeda Clinical Research (Veeda CR) is a leading clinical research organization (CRO) based in Ahmedabad, Gujarat. Known for its high standards and commitment to advancing clinical research, Veeda CR provides comprehensive services for clinical trials and bioanalytical research, maintaining a reputation for innovation and adherence to global standards. The company is highly regarded for its supportive culture and growth-oriented environment, making it an ideal place for professionals in bioanalytical research to launch or grow their careers. Analyst Bioanalytical Research at Veeda Clinical Research

Job Highlights

  • Work/Life Balance: Veeda CR emphasizes a balanced approach to professional responsibilities.
  • Time Management: Cultivate effective time management in a dynamic lab environment.
  • Flexibility & Problem Solving: Offers hands-on experience in addressing bioanalytical challenges.
    Analyst Bioanalytical Research at Veeda Clinical Research

Job Responsibilities

As an Analyst – Bioanalytical Research, you will play a critical role in supporting Veeda CR’s bioanalytical studies. This involves a range of technical and analytical tasks that contribute to the success of clinical trials and other research initiatives. Key responsibilities include: Analyst Bioanalytical Research at Veeda Clinical Research

1. Sample Preparation and Analysis

  • Assist in preparing and analyzing biological samples using bioanalytical techniques such as High-Performance Liquid Chromatography (HPLC), Liquid Chromatography-Mass Spectrometry (LC-MS/MS), and Enzyme-Linked Immunosorbent Assay (ELISA).
  • Ensure precise sample handling and preparation to maintain data accuracy and integrity.

2. Routine Laboratory Tasks

  • Conduct daily lab tasks such as handling samples, preparing reagents, and maintaining equipment.
  • Follow lab protocols to ensure all laboratory processes are conducted safely and efficiently.
    Analyst Bioanalytical Research at Veeda Clinical Research

3. Method Development and Troubleshooting

  • Support the method development and validation process, working closely with senior scientists.
  • Troubleshoot issues in sample preparation and analysis, providing insights for method improvement.

4. Data Collection and Documentation

  • Accurately record, collect, and analyze experimental data to support research findings.
  • Maintain thorough laboratory notebooks, ensuring documentation is clear, organized, and compliant with Veeda CR’s standards.

5. Regulatory Compliance

  • Adhere to laboratory safety protocols and regulatory standards to ensure quality and compliance in all research activities.
  • Stay updated on relevant regulations and best practices in bioanalytical research.
Analyst Bioanalytical Research at Veeda Clinical Research
Analyst Bioanalytical Research at Veeda Clinical Research

Responsibilities in Bioanalytical Quality Management (BQM)

In addition to core responsibilities, you may engage in quality management tasks:

  • Document Review: Review documents for accuracy, completeness, and regulatory compliance.
  • Report Monitoring: Oversee report preparation and archival processes, ensuring that documentation is secure and retrievable.
  • Data Monitoring: Perform quality checks on research data, upholding Veeda CR’s high standards of quality.
  • Audit Response and Compliance: Address audit-related queries and ensure compliance with established bioanalytical practices.
    Analyst Bioanalytical Research at Veeda Clinical Research

Qualifications and Skills Required

To excel in this role, candidates should possess the following qualifications and skills:

  • Educational Background: A bachelor’s or master’s degree in Life Sciences, Chemistry, Biotechnology, or a related field.
  • Experience: 0-3 years of experience in bioanalytical research or related laboratory work is preferred, though fresh graduates with a strong understanding of bioanalytical techniques are also encouraged to apply.
  • Technical Knowledge: Familiarity with bioanalytical techniques such as HPLC, LC-MS/MS, and ELISA.
  • Attention to Detail: Precision in handling and documenting lab activities.

Key skills that will support your role as an Analyst include:

  1. Analytical Skills: Ability to conduct and interpret bioanalytical tests accurately.
  2. Technical Proficiency: Experience with laboratory equipment and bioanalytical software is beneficial.
  3. Problem-Solving Skills: Aptitude for troubleshooting issues during method development.
  4. Communication Skills: Proficiency in both written and verbal communication, particularly for documentation and team collaboration.
  5. Regulatory Knowledge: Familiarity with laboratory safety standards and regulatory compliance protocols.
    Analyst Bioanalytical Research at Veeda Clinical Research
Analyst Bioanalytical Research at Veeda Clinical Research
Analyst Bioanalytical Research at Veeda Clinical Research

How to Apply

Interview Date: 10th November
Time: 9:30 AM to 2:00 PM
Venue: Satyamev Corporate, Corporate Rd, near Shalin Bungalows, Prahlad Nagar, Ahmedabad, Gujarat 380015.

To attend the interview, please bring:

  • Updated CV: Ensure your CV highlights relevant skills and any experience in bioanalytical techniques.
  • ID Proof and Academic Certificates: Bring your identification and relevant educational documents.
  • Preparedness for Discussion: Be ready to discuss any past laboratory work, research projects, or relevant academic experiences in detail.
    Analyst Bioanalytical Research at Veeda Clinical Research

Tips for Preparing for the Interview

  • Understand the Role: Review the job responsibilities and align your experience or knowledge with the specific requirements of bioanalytical research.
  • Highlight Relevant Skills: Be prepared to discuss any experience with HPLC, LC-MS/MS, or ELISA. Practical knowledge of these techniques will be an advantage.
  • Demonstrate Problem-Solving: Emphasize any situations where you solved lab-related challenges, as problem-solving is a valued skill at Veeda CR.
  • Showcase Documentation Skills: Discuss your approach to maintaining clear and detailed records, as attention to documentation is essential in this role.

About Veeda CR’s Work Culture

Veeda CR is recognized for its supportive and growth-driven work culture. Employees at Veeda CR often benefit from:

  • Mentorship and Training: Opportunities to work with senior scientists who provide guidance and support.
  • Career Growth: A work environment that fosters learning and advancement in bioanalytical research.
  • Collaborative Environment: Teamwork and collaboration are essential aspects of the work culture, providing an inclusive and professional environment for analysts.

Additional Job Highlights

Key FeatureDetails
SalaryCompetitive, based on experience
Work EnvironmentSupportive, growth-oriented
Interview Date10th November
LocationPrahlad Nagar, Ahmedabad, Gujarat
Time ManagementFlexible work conditions
DevelopmentSkill development in bioanalytical techniques

Takeaway: This is an excellent opportunity for recent graduates in life sciences, chemistry, or biotechnology to gain valuable experience in bioanalytical research at a leading CRO.

Analyst Bioanalytical Research at Veeda Clinical Research
Analyst Bioanalytical Research at Veeda Clinical Research

Associate Consultant Position at IQVIA

Associate Consultant Position at IQVIA

Associate Consultant Position at IQVIA

Job TitleAssociate Consultant
CompanyIQVIA
Experience Required2 – 3 Years
Salary Range8 – 12 Lacs per annum
LocationBangalore
Education RequirementsBachelor’s/Master’s in Life Sciences, Economics, Business, or Ph.D
Application ModeOnline
Job HighlightsWork/Life Balance, Flexibility, Problem Solving, Time Management
Key SkillsResearch & Analysis, Strategic Thinking, Client Interaction, Team Supervision, Proposal Development
Associate Consultant Position at IQVIA

Step into Healthcare Consulting as an Associate Consultant at IQVIA

The Associate Consultant role at IQVIA offers a unique opportunity to work closely with clients in the healthcare and life sciences sectors to address industry challenges, develop strategies, and deliver high-impact solutions. This full-time role based in Bangalore enables you to collaborate with a skilled team, gain valuable industry insights, and grow within a leading global healthcare consulting firm. Associate Consultant Position at IQVIA

Why Join IQVIA?

IQVIA is at the forefront of healthcare and life sciences consulting, providing valuable insights to clients through comprehensive research, analysis, and strategic recommendations. In this Associate Consultant position, you’ll not only engage in impactful projects but also enjoy a balanced work environment that emphasizes flexibility, work/life balance, and continuous learning. Associate Consultant Position at IQVIA

Role Overview

The Associate Consultant role involves extensive research and analysis to tackle client challenges, create actionable insights, and make strategic recommendations. You will work closely with clients, delivering solutions through presentations, reports, and workshops. Additionally, this role requires team supervision, client proposal assistance, and contributions to internal organizational activities. Associate Consultant Position at IQVIA


Key Responsibilities Breakdown

1. Research and Analysis

You’ll conduct primary and secondary research and utilize quantitative and qualitative analyses to gain insights into client issues. This will involve analyzing trends, synthesizing data, and deriving actionable strategies to address complex challenges in the healthcare and life sciences sectors. Associate Consultant Position at IQVIA

2. Strategic Recommendations

Your role requires you to leverage industry knowledge and business acumen to identify strategic alternatives. Developing actionable recommendations for clients is central to this position and will showcase your problem-solving abilities and understanding of client objectives. Associate Consultant Position at IQVIA

3. Client Interaction and Deliverables

You’ll collaborate closely with clients through presentations, workshops, and reports. Working alongside team members and leaders, you’ll help deliver projects that meet client expectations, providing them with the insights needed for strategic decisions.

4. Learning and Development

In addition to client work, you’ll have access to various learning and development opportunities that cover consulting methodologies and insights into the pharmaceutical market. This allows you to gain deeper knowledge while also enhancing your professional growth.

5. Team Supervision

As an Associate Consultant, you’ll oversee the work of junior team members on specific project deliverables. You’ll provide guidance and ensure high-quality outputs, helping to drive successful project outcomes.

6. Proposal Development

Assisting senior consultants in writing proposals is another key responsibility. This task provides exposure to the proposal development process and helps you learn how to convey value to potential clients effectively.

7. Client Meetings and Presentations

Supporting client meetings and presentations will be part of your role. Your involvement in delivering insights and discussing strategies helps reinforce the client’s confidence in IQVIA’s consulting services.

8. Organizational Contribution

Beyond client work, you’ll participate in team development and recruitment activities, contributing to the growth and success of the organization as a whole. Associate Consultant Position at IQVIA

Associate Consultant Position at IQVIA
Associate Consultant Position at IQVIA

Ideal Candidate Profile

IQVIA seeks candidates with a bachelor’s or master’s degree in life sciences, economics, business, or a Ph.D. in a relevant field. Candidates should bring 2-3 years of experience in healthcare/pharma or consulting, or relevant industry experience for Ph.D. holders. Associate Consultant Position at IQVIA

Desired Skills and Qualifications

  • Consulting Skills: Strong analytical and problem-solving skills, ideally with a background in commercial or strategy consulting.
  • Communication: Proficiency in report writing, presentation skills, and the ability to facilitate workshops with confidence.
  • Time Management: Ability to prioritize tasks effectively to meet multiple project deadlines.
  • Interpersonal Skills: A collaborative approach to working within teams to achieve shared goals.
  • Industry Knowledge: An understanding of trends and issues affecting the pharmaceutical and healthcare sectors.
  • Consulting Methodologies: Familiarity with consulting tools, techniques, and methodologies.
  • Adaptability and Learning: A demonstrated ability to learn and adapt quickly to new knowledge areas.
  • Travel Flexibility: Willingness to travel as required for project engagements. Associate Consultant Position at IQVIA

How to Stand Out as a Strong Candidate

To make a compelling case for this position:

  1. Showcase Industry Insight: Highlight any industry-specific experience or knowledge, particularly regarding current trends in healthcare and pharmaceuticals.
  2. Emphasize Analytical Skills: Discuss examples of past analytical projects where you developed insights or strategies based on quantitative and qualitative research.
  3. Communication and Client Skills: Mention your experience in presenting ideas, reports, or facilitating client workshops, demonstrating your ability to communicate effectively.
  4. Highlight Project Management Skills: Demonstrate your ability to handle multiple project components, deadlines, and team coordination.
  5. Share Examples of Adaptability: Highlight instances where you quickly learned new methodologies or adapted to different project demands.
Associate Consultant Position at IQVIA
Associate Consultant Position at IQVIA

Why This Role Could Be a Perfect Fit

The Associate Consultant role at IQVIA provides a unique opportunity to advance in healthcare consulting while working with a team that values collaboration, learning, and professional growth. You’ll play a key role in solving critical industry issues, gain exposure to leading industry practices, and enjoy a supportive environment where work/life balance and career progression are highly valued. Associate Consultant Position at IQVIA

This is a fantastic opportunity to make an impact in the healthcare consulting field, work with experienced consultants, and develop skills that will propel your career forward. If you’re ready to take on a role that blends strategy, client collaboration, and industry expertise, apply now to join IQVIA’s consulting team!

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Associate Consultant Position at IQVIA
Associate Consultant Position at IQVIA

PAREXEL Hiring for Principal Medical Writer Medical Writing Services

PAREXEL Hiring for Principal Medical Writer Medical Writing Services

PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Quick Reference for Principal Medical Writer Position

RolePrincipal Medical Writer, Medical Writing Services
CompanyPAREXEL
LocationBengaluru (Remote)
Experience Required10+ Years
EducationBachelor’s degree / Advanced degree in Life Sciences
Key SkillsRegulatory Writing, Project Management, Communication, Analytical Skills
Therapeutic ExpertiseVaccines, Immunology, Autoimmune, Cardiovascular, Neurology, Oncology
Application Deadline30th November 2024
Application ModeOnline
PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Join PAREXEL as a Principal Medical Writer – Make an Impact in Biopharma

PAREXEL, a global leader in biopharmaceutical services, is seeking an experienced Principal Medical Writer for its Medical Writing Services team. In this role, based remotely from Bengaluru, you will support PAREXEL’s mission to bring new therapies to market, impacting global healthcare positively. The role requires seasoned professionals with over 10 years of experience in regulatory medical writing, particularly in creating high-quality documents essential for clinical research and drug development. PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Why Choose PAREXEL?

PAREXEL offers a rewarding career in an organization dedicated to supporting the Bio-Tech and Pharmaceutical industries in developing life-changing treatments. Known for its innovative solutions and extensive global reach, PAREXEL provides an environment that promotes work-life balance, flexibility, and professional growth. If you are a passionate medical writer eager to make an impact, PAREXEL is the place to advance your career. PAREXEL Hiring for Principal Medical Writer Medical Writing Services

PAREXEL Hiring for Principal Medical Writer Medical Writing Services
PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Key Responsibilities of the Principal Medical Writer

As a Principal Medical Writer at PAREXEL, you will play a critical role in clinical documentation, project management, and client relations. Below are the primary responsibilities of this role: PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Clinical Research Document Creation

You’ll be responsible for creating, editing, and finalizing essential clinical documents, including protocols, clinical study reports, investigator’s brochures, informed consent forms, and summary documents. This work involves high-level writing skills and in-depth knowledge of regulatory requirements. PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Project Leadership and Client Engagement

As a project lead writer or submission coordinator, you’ll manage the contributions of multiple writers, ensuring cohesive, high-quality deliverables. You will serve as the primary point of contact for clients, communicating effectively to understand and meet their requirements. PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Process Improvement and Mentorship

PAREXEL values continuous improvement; thus, you’ll be instrumental in identifying and implementing process enhancements. In addition, you’ll provide mentorship and training to junior team members, nurturing a collaborative and growth-oriented work environment. PAREXEL Hiring for Principal Medical Writer Medical Writing Services

PAREXEL Hiring for Principal Medical Writer Medical Writing Services
PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Sales Support and Proposal Input

In collaboration with the sales and management teams, you’ll contribute to proposal development and client communications during the sales process, helping to align client needs with PAREXEL’s service offerings.

Ideal Candidate Profile

Experience:

  • At least 10 years of experience in regulatory medical writing within the biopharmaceutical or clinical research industry.
  • Proven expertise in authoring protocols, clinical study reports, and various regulatory documents.

Educational Background:

  • A bachelor’s degree in life sciences, healthcare, or a related field is required; an advanced degree is highly advantageous.

Skills and Competencies:

  • Regulatory Writing Expertise: Strong knowledge of regulatory requirements across therapeutic areas.
  • Project Management: Ability to independently lead projects, manage multiple timelines, and deliver on client expectations.
  • Communication and Interpersonal Skills: Clear and effective communication for both internal team coordination and client interaction.
  • Analytical Skills: Attention to detail and high accuracy in handling regulatory and clinical data.
  • Workload Management: Adaptability to manage varying workloads and meet deadlines without compromising quality.
    PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Therapeutic Area Expertise

This role requires knowledge across multiple therapeutic areas, including:

  • Vaccines
  • Immunology
  • Autoimmune Disorders
  • Cardiovascular Disorders
  • Endocrine Disorders
  • Gastrointestinal Disorders
  • Infectious Diseases
  • Mental Health
  • Neurology
  • Oncology

This broad therapeutic expertise allows the Principal Medical Writer to effectively support PAREXEL’s diverse client base in delivering accurate, insightful, and compliant clinical documentation.

Benefits of Working at PAREXEL

PAREXEL is committed to fostering a balanced work environment with ample opportunities for career advancement. Key benefits include:

  • Work/Life Balance: PAREXEL promotes a culture that supports work-life balance, ensuring you have flexibility in managing both personal and professional commitments.
  • Professional Development: The company offers ongoing training and development programs, supporting your continuous growth as a professional.
  • Collaborative Culture: You’ll work alongside industry experts, gaining insights and experience that contribute to your success as a medical writer.
    PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Apply Today

If you are a qualified, experienced medical writer ready to take on new challenges, consider joining PAREXEL as a Principal Medical Writer. This position not only provides the opportunity to make a significant contribution to the field of clinical research but also offers a flexible, rewarding work environment. Don’t miss your chance to work with a leader in biopharmaceutical services and contribute to innovations in global healthcare. PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Application Deadline: 30th November 2024. Start your journey with PAREXEL by applying online today and take the next step in your medical writing career.

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PAREXEL Hiring for Principal Medical Writer Medical Writing Services
PAREXEL Hiring for Principal Medical Writer Medical Writing Services

Drug Safety Associate (Pharmacovigilance) at Fortrea

Drug Safety Associate (Pharmacovigilance) at Fortrea

Drug Safety Associate (Pharmacovigilance) at Fortrea


Job Title: Drug Safety Associate (Pharmacovigilance)
Company: Fortrea
Location: [Insert Location]
Job Type: Full-time

About Us

Fortrea is a leading organization in the pharmaceutical industry, committed to ensuring the safety and efficacy of medications. We specialize in drug development and surveillance, providing comprehensive solutions that uphold the highest standards of patient safety. Our team is dedicated to fostering innovation and integrity in the field of pharmacovigilance, and we are looking for passionate individuals to join our dynamic workforce. Drug Safety Associate (Pharmacovigilance) at Fortrea

Position Overview

We are seeking motivated Freshers for the role of Drug Safety Associate (Pharmacovigilance) to join our team. This position is ideal for recent graduates who are looking to kickstart their careers in the pharmaceutical industry. As a Drug Safety Associate, you will play a vital role in monitoring and assessing the safety of pharmaceutical products, contributing to the overall mission of Fortrea to ensure patient safety and regulatory compliance. Drug Safety Associate (Pharmacovigilance) at Fortrea

Key Responsibilities

  • Adverse Event Reporting: Monitor, assess, and document adverse drug reactions (ADRs) and adverse events (AEs) reported by healthcare professionals and patients.
  • Data Entry and Management: Accurately enter safety data into our pharmacovigilance database, ensuring all entries comply with regulatory standards and internal procedures.
  • Case Processing: Review and process safety reports in accordance with established guidelines, ensuring timely submission to regulatory authorities.
  • Collaboration: Work closely with cross-functional teams including clinical operations, regulatory affairs, and medical affairs to ensure a comprehensive understanding of drug safety profiles.
  • Regulatory Compliance: Assist in the preparation of safety reports, ensuring adherence to local and international regulatory requirements.
  • Training and Development: Participate in training programs to enhance knowledge of pharmacovigilance practices, regulatory updates, and industry trends.
  • Quality Assurance: Support quality control processes by reviewing case files and ensuring compliance with SOPs and regulatory guidelines.
    Drug Safety Associate (Pharmacovigilance) at Fortrea

Qualifications

  • Educational Background:
  • Bachelor’s degree in Pharmacy (B.Pharm), Master’s degree in Pharmacy (M.Pharm), Doctor of Pharmacy (Pharm.D), Bachelor of Science (B.Sc), Master of Science (M.Sc), or other relevant qualifications in Life Sciences.
  • Skills:
  • Strong analytical and problem-solving skills.
  • Excellent attention to detail and organizational abilities.
  • Proficient in data entry and database management.
  • Strong verbal and written communication skills.
  • Ability to work collaboratively in a team-oriented environment.
  • Knowledge:
  • Basic understanding of pharmacovigilance principles and regulatory requirements is an advantage, but not mandatory for freshers.

Why Join Fortrea?

  • Career Growth: Fortrea is committed to the professional development of our employees. We offer comprehensive training programs and opportunities for career advancement within the organization.
  • Innovative Environment: Be a part of a forward-thinking company that values innovation and encourages employees to contribute their ideas and insights.
  • Work-Life Balance: We prioritize the well-being of our employees by promoting a healthy work-life balance and providing flexible working arrangements where possible.
  • Diverse Team: Join a diverse and inclusive workforce where different perspectives are valued and respected. Drug Safety Associate (Pharmacovigilance) at Fortrea

How to Apply

If you are excited about the opportunity to contribute to patient safety and the field of pharmacovigilance, we would love to hear from you! Please send your resume and a cover letter to the following number:

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Conclusion

At Fortrea, we believe that our employees are our greatest asset. We are looking for passionate and dedicated individuals who share our commitment to excellence in drug safety. If you are a recent graduate eager to make a difference in the pharmaceutical industry, apply today and embark on a fulfilling career with us! Drug Safety Associate (Pharmacovigilance) at Fortrea


Market Research Quality Analyst at GRG Health

Market Research Quality Analyst at GRG Health

Market Research Quality Analyst at GRG Health

Location: Pune and Gurugram
Experience: 0 Years
Salary: ₹3.5 Lakhs per year
Education: B.Pharm, M.Pharm, Bachelor’s or Master’s in Healthcare, Biotechnology, Microbiology, or Life Sciences

About GRG Health
GRG Health, part of the Growman Group, is a global leader in healthcare knowledge services and market research. With offices across India, Boston, and Singapore, we specialize in innovative machine learning models that drive insights in the healthcare sector. We’re looking for fresh graduates with a passion for healthcare and data analysis to join our dynamic team. Market Research Quality Analyst at GRG Health

Job Responsibilities

As a Market Research (Quality Analyst) at GRG Health, you will:

  • Conduct Quality Analysis: Utilize your expertise in biotechnology, biomedical sciences, and pharmaceuticals to ensure high-quality research content.
  • Recommend & Implement Improvements: Identify areas for quality improvement and implement preventive actions.
  • Ensure Content Accuracy: Maintain high standards of grammar, sentence flow, and structure for polished reports.
  • Effective Communication: Use excellent written and spoken communication to interact with team members and clients.
  • Use Microsoft Office: Leverage Microsoft Office applications (Word, Excel, PowerPoint) for report creation and presentations. Market Research Quality Analyst at GRG Health

Qualifications

We are looking for candidates with:

  • A Bachelor’s or Master’s degree in Healthcare, Biotechnology, Microbiology, or related Life Sciences streams.
  • Intermediate knowledge in Biotechnology, Biomedical, or Pharmaceutical fields.
  • Strong communication skills and proficiency in Microsoft Office.
  • Prior experience in healthcare market research is a plus but not mandatory.
    Market Research Quality Analyst at GRG Health
Market Research Quality Analyst at GRG Health
Market Research Quality Analyst at GRG Health

How to Apply

If you’re passionate about healthcare and excited to work in data analysis, send your CV to sweedal.fernandes@grgonline.com. Join GRG Health and contribute to the future of healthcare research!

Be a part of something extraordinary!

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Fresher Medical Documentation Specialist at Augmedix

Fresher Medical Documentation Specialist at Augmedix

Fresher Medical Documentation Specialist at Augmedix

Are you a recent graduate looking to begin a rewarding career in the healthcare sector? Do you have a passion for technology and healthcare but are unsure of where to start? If so, a role as a Medical Documentation Specialist at Augmedix could be the perfect fit for you! Fresher Medical Documentation Specialist at Augmedix

Augmedix is a leading healthcare technology company that is redefining how healthcare providers interact with medical documentation. They aim to transform the way doctors and patients experience healthcare by using innovative technology like remote scribing. Augmedix offers real-time medical documentation services that allow healthcare providers to focus more on patient care, streamline clinical workflows, and improve overall efficiency. With a growing demand for quality healthcare documentation, Augmedix stands at the forefront of healthcare innovation, helping providers deliver better care while maintaining accurate and efficient medical records. Fresher Medical Documentation Specialist at Augmedix

If you’re a fresher interested in a fast-paced, growth-oriented environment, this role provides an excellent opportunity to kick-start your career.

Why Choose Augmedix?

Augmedix is not just a company; it’s a mission-driven organization that seeks to enhance the healthcare experience for both providers and patients. The company’s core service is to assist healthcare providers by scribing medical documentation in real time during patient consultations. This allows doctors to give their full attention to patient care while Augmedix takes care of the documentation process. Augmedix is a trusted partner for healthcare institutions worldwide, offering innovative solutions that save time, reduce workload, and improve the accuracy of medical documentation. Fresher Medical Documentation Specialist at Augmedix

For freshers, Augmedix provides a platform where you can learn, grow, and excel in a dynamic and evolving field. As a Medical Documentation Specialist, you’ll play an essential role in the healthcare process, working closely with physicians and medical staff to ensure high-quality, accurate clinical documentation. Fresher Medical Documentation Specialist at Augmedix

Responsibilities of a Medical Documentation Specialist

As a Medical Documentation Specialist, your job is to support healthcare providers in documenting patient-provider interactions. This documentation is a vital part of the healthcare workflow, ensuring that all patient information is recorded accurately and efficiently. Below are some of the key responsibilities you will be tasked with: Fresher Medical Documentation Specialist at Augmedix

  1. Listening to Patient-Provider Interactions: Your primary role will be to listen to the conversations between doctors and patients, identifying important clinical details that need to be captured.
  2. Documenting Clinical Information: You will record relevant clinical information, such as symptoms, diagnoses, treatment plans, and medical histories, in an organized manner.
  3. Ensuring Accuracy and Quality: You must ensure that all the information you document is accurate, complete, and free of errors. Medical documentation is crucial for patient care, and even minor mistakes can have significant consequences.
  4. Maintaining Confidentiality: You will be handling sensitive patient information, so maintaining confidentiality and following healthcare compliance guidelines (such as HIPAA) is non-negotiable.
  5. Collaborating with Doctors: You’ll work closely with healthcare providers to create well-organized and compliant documentation. This collaboration will enhance the quality and efficiency of patient care.
  6. Updating Electronic Health Records (EHR): As part of your daily tasks, you will update Electronic Health Records (EHR) in real time, ensuring that all patient data is current and readily available for healthcare providers. Fresher Medical Documentation Specialist at Augmedix
Fresher Medical Documentation Specialist at Augmedix
Fresher Medical Documentation Specialist at Augmedix

Qualifications Required for the Role

This is a fantastic opportunity for freshers, as no prior work experience is required. However, certain qualifications and skills will make you a good fit for the position:

  1. Educational Background: You should have a bachelor’s degree in any discipline, though candidates with degrees in Life Sciences, Pharmacy, Pharm.D, or related fields are preferred. If you have a foundational understanding of healthcare or medical sciences, this will be an added advantage.
  2. Medical Terminology: A basic understanding of medical terminology is preferred but not mandatory. If you’re not familiar with medical terms, don’t worry—training will be provided to ensure you’re well-equipped for the job.
  3. Typing Speed & Computer Literacy: Good typing speed is essential, as you’ll be required to document interactions in real-time. You should also be familiar with using computers and data entry tasks.
  4. Willingness to Learn: Since this is a healthcare environment, things can move quickly. You should be willing to learn new skills and adapt to a fast-paced, ever-changing work environment. Fresher Medical Documentation Specialist at Augmedix

Skills Needed to Excel in this Role

To succeed in this role, several key skills are essential. These skills will not only help you perform your daily tasks efficiently but will also ensure that you stand out as a valuable member of the Augmedix team: Fresher Medical Documentation Specialist at Augmedix

  1. Excellent Communication Skills: Since you’ll be listening to patient-provider conversations, it’s important that you have strong communication skills. You’ll need to understand these conversations clearly, especially when documenting critical medical details.
  2. Attention to Detail: Medical documentation requires a high degree of accuracy. Even the smallest error could lead to incorrect medical records, which could have serious consequences. Your ability to focus on the finer details will be a key factor in ensuring that records are accurate and reliable.
  3. Time Management: The healthcare environment is fast-paced, and there will be multiple tasks to handle throughout the day. Being able to manage your time efficiently will help you keep up with the demands of the job. Fresher Medical Documentation Specialist at Augmedix
  4. Basic Computer Skills: You’ll need to be proficient in using Electronic Health Records (EHR) software and handling data entry tasks. Basic computer literacy is crucial for this role.
  5. Confidentiality & Compliance: Handling sensitive patient data requires a strong sense of responsibility and adherence to compliance guidelines. You must be diligent about maintaining confidentiality at all times. Fresher Medical Documentation Specialist at Augmedix
Fresher Medical Documentation Specialist at Augmedix
Fresher Medical Documentation Specialist at Augmedix

How to Apply for the Role

If you’re excited about the opportunity to begin your career with a company that’s transforming the healthcare industry, apply now to become a Medical Documentation Specialist at Augmedix! This role is ideal for freshers who are ready to learn, adapt, and contribute to a dynamic team.

To apply, send your updated resume to the following email addresses:

  • srikumar.bhaskaran@augmedix.com
  • careers-india@augmedix.com

In your email, be sure to include the subject line:
“Application for Medical Documentation Specialist | Fresher”.

This is your chance to work in an innovative and fast-growing healthcare company, gain invaluable experience, and take the first step toward a promising career in medical documentation. Join Augmedix today and be part of a team that’s changing the future of healthcare!

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