Bachelor’s/Master’s

Pharmacovigilance Hiring at Accenture

November 16, 2024 by Ranjeet kashyap

Pharmacovigilance Hiring at Accenture

Key Points for Job Seekers

Details	Information
Position	Pharmacovigilance Services Associate
Company	Accenture
Experience Required	0 – 1 year
Salary Range	₹4,00,000 – ₹7,00,000 per year
Location	Bangalore
Job Type	Full-Time
Educational Qualifications	Bachelor of Pharmacy (B.Pharm)
Job Highlights	Work-Life Balance, Time Management, Flexibility, Problem Solving
Responsibilities	Mailbox Management, Case Processing, MedDRA Coding, Timely ICSR Submissions
Skills Required	Attention 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

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:

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

November 12, 2024 by Ranjeet kashyap

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

Feature	Details
Work/Life Balance	Supportive and flexible environment
Time Management	Emphasis on effective time utilization
Flexibility	Adaptability to production demands
Problem Solving	Encouraged 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

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

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!

Lab Report Coordinator Intern at ICON Plc

November 10, 2024 by Ranjeet kashyap

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

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.

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.

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.

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

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

Understand the Role: Review the job responsibilities to understand the specific duties and challenges of lab report coordination.
Highlight Relevant Skills: Be prepared to discuss your knowledge of laboratory information systems and your experience (if any) in data entry tasks.
Demonstrate Problem-Solving Abilities: Emphasize any relevant experience or coursework that demonstrates your ability to identify and correct errors or discrepancies.
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 Feature	Details
Position	Lab Report Coordinator Intern
Location	Bangalore, India
Experience Required	0-1 year
Skills Emphasized	Data accuracy, communication, problem-solving
Application Mode	Online Application
Education Required	B.Sc. MLT or related field

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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.

Associate Consultant Position at IQVIA

November 6, 2024 by Ranjeet kashyap

Associate Consultant Position at IQVIA

Job Title	Associate Consultant
Company	IQVIA
Experience Required	2 – 3 Years
Salary Range	8 – 12 Lacs per annum
Location	Bangalore
Education Requirements	Bachelor’s/Master’s in Life Sciences, Economics, Business, or Ph.D
Application Mode	Online
Job Highlights	Work/Life Balance, Flexibility, Problem Solving, Time Management
Key Skills	Research & 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

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:

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

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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Research Associate / Senior Research Associate at INTOX

October 27, 2024 by Ranjeet kashyap

Research Associate / Senior Research Associate at INTOX

Key Highlights

Position	Research Associate / Senior Research Associate
Location	Pirangut, Pune
Experience	4-5 years
Education	Master’s or Ph.D. in Toxicology, Molecular Biology, Biotechnology, or related field
Department	Toxicology / Genotoxicology
Skills	Genotoxicology Assays, GLP Compliance, Data Analysis, Regulatory Submissions
Job Type	Walk-In Interview
Application Email	varsha.khande@intoxlab.com

Research Associate / Senior Research Associate at INTOX

Unlock Your Potential in Toxicology with INTOX

Are you passionate about advancing your career in toxicology or genotoxicology? INTOX is offering an exciting opportunity for a Research Associate or Senior Research Associate to join our dynamic team at Pirangut, Pune. This role is perfect for professionals with 4-5 years of experience, looking to expand their skills in a GLP-compliant environment. Research Associate / Senior Research Associate at INTOX

What You Will Do

At INTOX, you’ll have the chance to make a real impact through the following responsibilities:

Conduct Genotoxicology Studies: You’ll carry out a variety of genotoxicology assays like the Ames test, Micronucleus test, and Comet assay, ensuring that the data gathered is accurate and actionable.
Data Analysis and Interpretation: Your role will involve analyzing and interpreting complex datasets, helping your team make informed decisions that drive scientific progress.
Ensure GLP Compliance: You’ll be at the forefront of ensuring all laboratory processes comply with GLP (Good Laboratory Practice), maintaining top-notch documentation for every project.
Collaborate with Experts: Work closely with team members and contribute to cross-functional projects, ensuring that all studies meet stringent quality and regulatory standards.
Prepare Regulatory Submissions: Be involved in drafting submissions for regulatory bodies, helping to secure approvals for groundbreaking research.
Research Associate / Senior Research Associate at INTOX

Why INTOX?

Working at INTOX offers a balanced lifestyle with a focus on:

Work/Life Balance: We believe that maintaining a healthy balance is crucial for optimal performance and job satisfaction.
Flexibility: The role allows for flexibility in managing your time and responsibilities.
Problem-Solving Environment: You’ll be part of a culture that encourages innovation and finding solutions to complex scientific challenges.
Research Associate / Senior Research Associate at INTOX

Qualifications We’re Looking For

To be successful in this role, you’ll need:

A Master’s or Ph.D. in Toxicology, Molecular Biology, Biotechnology, or a related field.
4-5 years of hands-on experience in a GLP-compliant lab, especially working with genotoxicology assays.
Strong knowledge of OECD guidelines and regulatory requirements in the field.

How to Apply

Excited to be part of our cutting-edge team? We’d love to hear from you! Walk into our interview or send your resume to varsha.khande@intoxlab.com today.

Take the next step in your career with INTOX and help shape the future of toxicology research!

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Fresher Hiring Project Associate I at IQVIA

October 18, 2024 by Ranjeet kashyap

Fresher Hiring Project Associate I at IQVIA

IQVIA is a global leader in clinical research, healthcare intelligence, and commercial insights, dedicated to improving patient outcomes and public health worldwide. As a Project Associate I at IQVIA, based in Bengaluru, Karnataka, India, you will have the opportunity to work at the forefront of medical innovation. With a Bachelor’s or Master’s degree in life sciences or a related field, this full-time role offers an entry point to a rewarding career in healthcare and project management. Fresher Hiring Project Associate I at IQVIA

Here’s a quick overview of the job’s key points to help you understand the position easily:

Position	Project Associate I at IQVIA
Location	Bengaluru, Karnataka, India
Job Type	Full-Time
Education Requirement	Bachelor’s/Master’s degree in life sciences, project management, or related field
Years of Experience	0 years (entry-level)
Key Skills	Data management, problem-solving, project coordination, documentation
Workplace Highlights	Work/Life balance, flexibility, problem-solving, and time management
Salary	Not disclosed

Fresher Hiring Project Associate I at IQVIA

Why IQVIA?

IQVIA is at the intersection of data, technology, and life sciences, empowering healthcare organizations worldwide to make more informed decisions. Whether you’re a recent graduate or transitioning into the field of project management, IQVIA provides a platform for career growth, where you’ll collaborate with teams to accelerate the development of medical treatments that enhance patient care.
Fresher Hiring Project Associate I at IQVIA

Key Responsibilities

As a Project Associate I, you will play a crucial role in supporting project coordination, data management, and study closeouts. The position involves handling a variety of responsibilities, including:

1. Data Changes (50%)

Your primary focus will be managing data change requests based on client requirements. This involves creating and coordinating data updates and changes, ensuring they are implemented correctly and on time. You will work closely with various teams to guarantee smooth data operations, making this role essential to the overall success of ongoing projects.
Fresher Hiring Project Associate I at IQVIA

2. Maintenance Tasks (30%)

You will also manage maintenance tasks, including handling tickets related to issue investigation and resolution. Unresolved problems will be escalated to appropriate teams, ensuring that all aspects of the project stay on track. This is your chance to contribute to various stages of project execution, from data setup to ticket management and problem-solving.

3. Documentation (15%)

In this role, you’ll be responsible for preparing essential project documentation, such as study-specific user guides. You’ll receive feedback from project managers to create and finalize critical documents and assist in creating presentation slides or updating communication tools. Attention to detail and strong writing skills will be your keys to success. Fresher Hiring Project Associate I at IQVIA

4. Closeout Tasks (5%)

When a study concludes, you’ll perform study closeout checks to ensure all necessary processes have been completed correctly. Your work in documenting and downloading reports will be critical for the project’s final wrap-up and will serve as a reference for future initiatives.

5. Ad-hoc Tasks

Your flexibility and adaptability will come into play with ad-hoc duties, where you will tackle additional tasks as needed. This could involve working with different departments or diving into new challenges that arise, offering you the chance to broaden your skillset and experience.

Qualifications and Skills Required

To excel in this role, IQVIA is looking for individuals with a Bachelor’s or Master’s degree in life sciences, project management, or a related field. While experience in data management or project coordination is beneficial, it is not mandatory. Your ability to problem-solve, coordinate across teams, and manage project documentation will make you an invaluable asset to the IQVIA team. Fresher Hiring Project Associate I at IQVIA

Additional skills that will set you apart include:

Excellent communication skills for working with internal teams and clients
Proficiency in documentation and using tools like SharePoint
A keen eye for detail and a knack for handling data-related tasks efficiently
Fresher Hiring Project Associate I at IQVIA

Why Choose This Role?

This role is perfect for those seeking an entry point into the dynamic world of healthcare and clinical research. IQVIA is not just offering a job; it’s offering career development, global impact, and the chance to be part of something bigger. With an emphasis on work/life balance, flexibility, and problem-solving, this role ensures that you’ll grow both professionally and personally.

Take this opportunity to launch your career at IQVIA and make a real difference in the healthcare industry!

Apply now and be part of the revolution in medical innovation. Fresher Hiring Project Associate I at IQVIA

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PV Validation Analyst at 3Analytics

October 17, 2024 by Ranjeet kashyap

PV Validation Analyst at 3Analytics

Experience: 3 Years
Salary: ₹4 – 8 Lacs Per Year
Location: Remote
Education: Bachelor’s degree in Life Sciences, Computer Science, Engineering, or a related field

Why Join 3Analytics?

3Analytics is a forward-thinking company specializing in providing pharmacovigilance and validation services. As a PV Validation Analyst, you’ll play a critical role in ensuring that pharmacovigilance systems meet regulatory standards. Working with a remote team of experts, this position offers flexibility, work-life balance, and the opportunity to contribute to the safety and efficacy of pharmaceutical products. PV Validation Analyst at 3Analytics

Position Overview: PV Validation Analyst

The PV Validation Analyst will be responsible for conducting thorough Computer System Validation (CSV) activities to ensure compliance with regulatory requirements, including 21 CFR Part 11 and EU Annex 11. You will work closely with various teams to manage validation documentation, ensure compliance, and tackle issues within the pharmacovigilance (PV) systems. PV Validation Analyst at 3Analytics

Key Responsibilities

Validation Documentation: Develop and review validation plans, protocols, and reports for CSV activities, ensuring that documentation is accurate and up to regulatory standards.
Compliance Assurance: Ensure pharmacovigilance systems comply with 21 CFR Part 11, EU Annex 11, and other relevant regulations.
Problem Solving: Identify issues related to PV systems and work independently to resolve them with minimal supervision.
Project Management: Manage multiple validation tasks efficiently, meeting project deadlines without compromising quality.
Collaboration: Work with cross-functional teams, including IT, quality assurance, and pharmacovigilance departments, to ensure seamless validation processes. PV Validation Analyst at 3Analytics

Required Qualifications

Education: A Bachelor’s degree in Life Sciences, Computer Science, Engineering, or a related field.
Experience: A minimum of 3 years of experience in Computer System Validation (CSV) within the pharmaceutical or pharmacovigilance industry.
Regulatory Knowledge: A strong understanding of 21 CFR Part 11 and EU Annex 11, with the ability to apply these regulations to PV systems.
Skills:
Expertise in creating, reviewing, and managing validation documentation.
Strong attention to detail and the ability to work independently.
Problem-solving skills, with the ability to handle multiple tasks efficiently.
Excellent communication and interpersonal skills to collaborate with diverse teams.
PV Validation Analyst at 3Analytics

Preferred Qualifications

PV System Experience: Familiarity with pharmacovigilance systems such as Argus, ArisGlobal, or similar tools is highly preferred.
Risk Management: Expertise in identifying risks and implementing mitigation strategies during CSV activities.
GxP Knowledge: Solid understanding of GxP regulations and their application within a pharmacovigilance context.

What We Offer

At 3Analytics, we offer a supportive and flexible work environment where your expertise will contribute to the success of innovative projects. You’ll have the opportunity to grow professionally, enjoy work-life balance, and work remotely with a team that values collaboration and innovation. PV Validation Analyst at 3Analytics

How to Apply

If you have the relevant experience and are ready to take on a challenging yet rewarding role in PV validation, we encourage you to apply!

Apply online to become a part of 3Analytics and make a difference in the world of pharmacovigilance and compliance.

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Mudra Clincare Hiribg for Clinical Research

October 17, 2024 by Ranjeet kashyap

Mudra Clincare Hiribg for Clinical Research

Mudra Clincare is a leading clinical research center known for its innovative approach to healthcare. We are excited to expand our team with dynamic individuals who are passionate about clinical research. If you’re looking to enhance your career in the healthcare industry and want to be part of a vibrant, forward-thinking team, this opportunity is for you! Mudra Clincare Hiribg for Clinical Research

Key Details at a Glance

Position	Experience	Qualification	Location
Clinical Trial Assistant (CTA)	1 Year	Masters in Clinical Research, Life Science, B.Pharm	Navi Mumbai
Clinical Research Associate (CRA)	Minimum 1 Year	Masters in Clinical Research, Life Science, B.Pharm	Navi Mumbai
Clinical Research Coordinator (CRC)	1-4 Years	B.Pharm, M.Pharm, Nursing, Pharm.D, Life Sciences, Clinical Research	Navi Mumbai

Mudra Clincare Hiribg for Clinical Research

Number of Openings: 02
Compensation: As per industry norms
Location: Navi Mumbai, office-based role

Why Join Mudra Clincare?

At Mudra Clincare, we believe that every member of our team plays a pivotal role in advancing healthcare through cutting-edge clinical research. Joining us means you’ll work in an environment that fosters collaboration, innovation, and personal growth. If you’re ready to dive into exciting projects and take on meaningful challenges, this is the perfect place for you.

Work-Life Balance & Flexibility

We understand the importance of maintaining a healthy work-life balance, especially in a fast-paced field like clinical research. At Mudra Clincare, we prioritize flexible working hours and the ability to manage your time effectively. This allows you to excel in your role while ensuring personal well-being and development. Mudra Clincare Hiribg for Clinical Research

Problem Solving & Growth Opportunities

Our team is dedicated to finding creative solutions in the ever-evolving world of clinical research. As part of Mudra Clincare, you’ll be encouraged to think outside the box, approach challenges with a problem-solving mindset, and contribute to the overall success of our projects. We are committed to providing you with continuous learning opportunities, allowing you to grow and stay at the forefront of the industry. Mudra Clincare Hiribg for Clinical Research

Available Positions

1. Clinical Trial Assistant (CTA)

As a Clinical Trial Assistant, you will play a crucial role in ensuring the smooth execution of clinical trials. You’ll assist with trial documentation, manage timelines, and communicate with different departments to facilitate trial success. With a strong focus on time management and organizational skills, this position is ideal for someone looking to start their career in clinical research. Mudra Clincare Hiribg for Clinical Research

Experience Required: 1 year
Qualification:

Masters in Clinical Research
Masters in Life Science
B.Pharm or other relevant degrees

2. Clinical Research Associate (CRA)

As a Clinical Research Associate, you’ll be responsible for monitoring clinical trials and ensuring that they are conducted in compliance with regulatory requirements. You will also interact with trial sites, review data, and support investigators. If you have a passion for ensuring clinical trials run smoothly and are ready for the next step in your career, this role is perfect for you. Mudra Clincare Hiribg for Clinical Research

Experience Required: Minimum 1 year
Qualification:

Masters in Clinical Research
Masters in Life Science
B.Pharm or other relevant degrees

3. Clinical Research Coordinator (CRC)

This role involves managing the day-to-day activities of clinical research trials. As a Clinical Research Coordinator, you will ensure that clinical research protocols are followed, trials are conducted efficiently, and data is collected accurately. The position is perfect for someone who thrives in a structured environment and enjoys overseeing trial operations. Mudra Clincare Hiribg for Clinical Research

Experience Required: 1-4 years
Qualification:

B.Pharm, M.Pharm
Nursing
Pharm.D
Life Sciences
Clinical Research

How to Apply

Are you excited to be part of the future of healthcare? If you meet the qualifications and are ready for immediate joining, we want to hear from you!

📧 Send your resume to:

mudraclincare@gmail.com
info@mudraclincare.org

At Mudra Clincare, we’re looking for talented individuals who can make an impact in clinical research. Join us today and be part of a team that’s transforming healthcare!

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Intern Opportunity at Medtronic

October 14, 2024 by Ranjeet kashyap

Intern Opportunity at Medtronic

Position	Intern
Location	Mumbai
Experience	0 Years (Freshers Welcome)
Stipend	Available
Education	Bachelor’s Degree
Application Mode	Online
Key Highlights	Work/Life Balance, Time Management, Flexibility, Problem Solving

Transform Healthcare with Medtronic

At Medtronic, we believe in pushing the boundaries of innovation to transform healthcare. With over 90,000 employees across the globe, we are dedicated to bringing bold ideas to life, alleviating pain, restoring health, and extending lives. This internship provides you with the unique opportunity to be part of our mission and help shape the future of healthcare. If you’re looking for an exciting start to your career where you can make a real impact, this is the perfect role for you. Intern Opportunity at Medtronic

A Day in the Life – Your Key Responsibilities

As a Medtronic intern, you’ll be joining a dynamic, fast-paced environment where you’ll get hands-on experience and contribute to important projects. Your role will involve working with various teams, including service groups, product teams, or specific project teams, to collaborate and support business needs. Here’s what you can expect to do on a daily basis: Intern Opportunity at Medtronic

Collaborate with Teams: You’ll be working alongside professionals from different departments such as sales, marketing, and business development, gaining insight into the industry and building knowledge that will set you up for success.
Project Assistance: Assist in developing, coordinating, monitoring, and implementing various projects. Your role will be crucial in ensuring projects run smoothly and meet objectives.
Research & Reporting: Conduct quantitative and qualitative research, industry analysis, and contribute to reports. Your findings will help the team make data-driven decisions.
Identify Process Improvements: Look for opportunities to improve existing processes and suggest new projects that could enhance business outcomes.
Cross-Departmental Interaction: Participate in communication efforts and support cross-departmental tasks, helping to foster collaboration within the organization.
Intern Opportunity at Medtronic

Specialist Career Stream – Grow with Medtronic

This internship falls under the Specialist Career Stream, where you’ll take on the role of an individual contributor. Your focus will be on delivering and managing your assigned projects while working closely with other stakeholders to meet the company’s goals. You’ll also have the opportunity to mentor junior colleagues and manage smaller-scale initiatives, giving you the chance to develop leadership skills early on in your career. Intern Opportunity at Medtronic

Why This Internship is Perfect for You

Problem-Solving Skills

At Medtronic, we value individuals who can think critically and solve minor issues within systems and processes. Your ability to identify and address problems will help you thrive in this internship. Intern Opportunity at Medtronic

Communication is Key

Good communication is crucial to success in this role. You’ll need strong interpersonal skills to work effectively within internal teams and collaborate across different departments.

Self-Motivation and Growth

We’re looking for self-motivated individuals who are driven to learn and grow. In this internship, you’ll have plenty of opportunities for personal and professional development, helping you build a solid foundation for your career. Intern Opportunity at Medtronic

Required Skills and Qualifications

To qualify for this exciting opportunity, here’s what we’re looking for:

Education: A Bachelor’s degree (or equivalent degree meeting global standards) is required. Whether you’ve just graduated or are about to, this role is open to freshers with no prior work experience.
Competencies: You should have a strong desire to learn, excellent problem-solving skills, and the ability to communicate effectively with teams.

Application link

Why Choose Medtronic?

Medtronic is committed to fostering a culture of innovation, collaboration, and care. By joining our team, you’ll be part of a company that is passionate about making a difference in people’s lives. From working on cutting-edge projects to building industry knowledge and improving your skills, this internship will equip you with everything you need to succeed in your future career.

This is your chance to be part of something bigger—helping to shape a more connected, compassionate, and innovative healthcare system. Start your journey with Medtronic today!