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Pharmacovigilance Hiring at Accenture

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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

Data Analyst Position at Gainwell Technologies

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Data Analyst Position at Gainwell Technologies

Data Analyst Position at Gainwell Technologies

PositionData Analyst
CompanyGainwell Technologies
LocationBangalore
Experience1+ years, freshers considered for specific roles
Salary₹3 Lakhs per year
QualificationB.Pharm, M.Pharm, Pharm.D, MSc, BSc, Life Sciences
SkillsSQL, data mapping, healthcare processes
Work EnvironmentHybrid, with work-life balance focus
ApplicationOnline
Data Analyst Position at Gainwell Technologies

Join Gainwell Technologies as a Data Analyst and Make a Difference in Healthcare

Are you looking to use your analytical skills in a role where technology meets healthcare to bring about meaningful change? Gainwell Technologies is hiring a Data Analyst in Bangalore, and this position is your opportunity to be part of an innovative team tackling some of healthcare’s most pressing issues. As a Data Analyst, you’ll be responsible for mapping and supporting key data processes, contributing directly to improving health outcomes for underserved communities. Data Analyst Position at Gainwell Technologies

Why Work at Gainwell Technologies?

Gainwell is dedicated to addressing the healthcare needs of vulnerable populations by leveraging advanced technology and data solutions. By joining Gainwell, you’ll be working in a field that blends technology with healthcare, helping you build a career in a dynamic and rewarding sector. Here’s what makes Gainwell an excellent place to work: Data Analyst Position at Gainwell Technologies

  • Mission-Driven: Gainwell focuses on improving the lives of underserved communities.
  • Growth and Learning: Gain valuable experience in healthcare-related data processes and develop expertise in ETL, data mapping, and healthcare analytics.
  • Supportive Work Environment: Gainwell promotes work-life balance and offers a hybrid work model to accommodate flexibility.
  • Fast-Paced: Expect an engaging, fast-moving work environment that encourages continuous improvement and innovation.

Your Responsibilities as a Data Analyst

As a Data Analyst, you’ll take on various tasks essential to the healthcare data infrastructure Gainwell relies on. Here’s a closer look at what you’ll be doing: Data Analyst Position at Gainwell Technologies

1. Mapping Documentation

  • Create and maintain precise mapping documents, a crucial part of Gainwell’s data infrastructure.
  • Follow established mapping processes to ensure accuracy and consistency, providing a foundation for data integrity and seamless operations. Data Analyst Position at Gainwell Technologies
Data Analyst Position at Gainwell Technologies
Data Analyst Position at Gainwell Technologies

2. ETL/Reporting/Conversion Support

  • Assist ETL, reporting, and conversion developers by drafting solutions and mapping details.
  • Your support helps developers execute their tasks effectively, ensuring the end-to-end data pipeline runs smoothly.

3. Collaborate with Teams

  • Work closely with Gainwell’s configuration team and database administrators (DBAs) to align configuration details and mappings.
  • This collaboration ensures smooth synchronization across teams, enhancing the accuracy and efficiency of data flows. Data Analyst Position at Gainwell Technologies

4. Research and Analysis

  • Conduct thorough research to inform data mapping and design mapping documents that support business requirements.
  • Present findings and suggest best practices to team members, clients, and vendors, making a real impact on healthcare data processes.

Skills and Qualifications Needed

To thrive in the Data Analyst role at Gainwell, here’s what you’ll need:

Healthcare Data Knowledge

Familiarity with healthcare processes and data is crucial. Key concepts include:

  • Member Eligibility: Knowing how eligibility data is processed and managed.
  • Third-Party Liability (TPL): Understanding how third-party claims affect healthcare providers and payers.
  • Claims Processing: Familiarity with provider and pharmacy claims, a core part of healthcare data.

SQL and Data Mapping

  • SQL Proficiency: Strong SQL skills for data manipulation, extraction, and analysis are essential.
  • Data Mapping Experience: Experience in data mapping is a key qualification for this role.
  • Background in Conversion, Interface, or Reporting: This experience is beneficial and enhances your suitability for this role.
  • Knowledge of QXNT: While not mandatory, familiarity with the QXNT platform is a plus.
    Data Analyst Position at Gainwell Technologies

Soft Skills for Success

Gainwell values candidates who can communicate effectively, problem-solve, and collaborate within a team. Essential skills include:

  • Communication: Excellent oral and written communication skills for sharing insights and collaborating with others.
  • Problem Solving: A solution-oriented mindset to troubleshoot and resolve data issues.
  • Team Collaboration: Strong ability to work in a team environment, contributing positively to Gainwell’s mission.
Data Analyst Position at Gainwell Technologies
Data Analyst Position at Gainwell Technologies

What You Can Expect from Gainwell Technologies

Gainwell offers an environment that’s not only challenging but also supportive and accommodating. Here’s what you can look forward to:

  • Pace and Challenges: Gainwell’s dynamic work culture requires adaptability and a readiness to tackle challenges, making every day unique.
  • Work-Life Balance: Gainwell emphasizes work-life balance, providing a hybrid model that allows you to work remotely on designated days.
  • Late Evening Hours: Some overlap with U.S. work hours may be needed, so be prepared for evening work.

How to Apply

To apply for the Data Analyst position, visit Gainwell’s official career portal and complete the online application. If you’re passionate about healthcare and data analytics, don’t miss this opportunity to be part of a team making a difference.

Take Your Next Career Step with Gainwell Technologies

As a Data Analyst at Gainwell Technologies, you’ll work at the forefront of healthcare data analytics, gaining experience that can shape a meaningful and impactful career. From creating essential mapping documents to collaborating with teams on healthcare data processes, this role provides a unique chance to apply your analytical skills while contributing to a greater cause. Data Analyst Position at Gainwell Technologies

See This Jobs – Health Operations New Associate at Accenture

Start your journey with Gainwell Technologies and make a positive impact on healthcare. Apply today and become a part of a team dedicated to transforming healthcare through technology!

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Head – Business Development/Placement Manager at ISME

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Job Posting: Head – Business Development/Placement Manager

Position Name: Head – Business Development/Placement Manager

Company Name: International School of Management Excellence (ISME)

Department: Business Development/Placement

Qualification: Post-graduation in management or equivalent

Experience: Minimum 12+ years in placements, corporate relations, recruitment consulting, or marketing MDP/consulting projects

Job Location: Domasandra Circle, Sarjapura Rd, Bangalore

E-Mail: jobs@isme.in

About ISME:
ISME is a top B-School in Bangalore offering BBA, BCom, PGDM, and PhD programs. We are AICTE approved and NBA accredited.

Position: Head – Business Development/Placement Manager

Responsibilities:

  • Strategy & Growth:
  • Drive business development strategies
  • Enhance current portfolio and explore new growth opportunities
  • Industry Partnerships:
  • Establish and maintain productive industry partnerships
  • Generate employment opportunities for students
  • Marketing Initiatives:
  • Plan and oversee new marketing initiatives
  • Research:
  • Research organizations and individuals for new business and placement opportunities
  • Client Relations:
  • Develop and nurture relationships with clients and corporates
  • Strengthen industry partnerships
  • Programs:
  • Facilitate and promote executive development and consulting programs

Requirements:

QualificationExperienceSkills
Post-graduation in management or equivalentMinimum 12+ years in placements, corporate relations, recruitment consulting, or marketing MDP/consulting projectsGood corporate contacts and networking skills
Excellent communication skills

Additional Requirement:

  • Candidates must reside within 20 kms of ISME campus or be willing to relocate nearby.

How to Apply:
Send your resume to

Resume Now

Note: This format is structured for easy readability and ensures that important details are highlighted effectively.

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ResMed Hiring for Regulatory Affairs Administrative Assistant

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ResMed Hiring for Regulatory Affairs Administrative Assistant

About ResMed:
ResMed’s products must comply with regulatory requirements for medical devices in various global markets, including the FDA (USA), competent authorities in Europe, and the TGA (Australia). Our products are known for high-quality standards, performance, and reliability.

Position:

  • Title: Regulatory Affairs Administrative Assistant
  • Department: Regulatory Affairs

Organization:

  • ResMed

Qualifications:

  • B.Pharm, M.Pharm, M.Sc, B.Sc

Experience:

  • 1 to 2 Years

Salary:

  • ₹25,000 – ₹35,000 /month

Location:

  • Bangalore
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Job Responsibilities:

TaskDescription
Document ManagementAssist in preparing, compiling, and maintaining regulatory documentation, including submissions, forms, reports, and records.
CommunicationHandle administrative requests and queries related to regulatory matters.
Meeting CoordinationSchedule and organize meetings, including taking detailed minutes during regulatory discussions.
Filing SystemDevelop and maintain an organized filing system for regulatory documents, including updates to tracking systems.
Policy UpdatesAssist in updating and maintaining policies and procedures related to regulatory affairs.
LiaisonAct as a point of contact for internal and external stakeholders regarding regulatory inquiries.

How to Apply:
Join ResMed’s regulatory affairs team and support our mission to maintain high standards in medical device compliance. Apply now!

Application Link

Meta Description:
ResMed hiring Regulatory Affairs Administrative Assistant in Bangalore. Apply now with 1-2 years experience in Pharma/Science.

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TCS Hiring in Clinical Data Management In Mumbai, Pune, Bangalore

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TCS Hiring in Clinical Data Management In Mumbai, Pune, Bangalore

About TCS:
TCS Interactive Life Sciences delivers comprehensive solutions for enhanced patient engagement and outcomes.

Position:
Data Manager / Senior Data Manager

Organization:
TCS

Location:
Mumbai, Pune, Bangalore

Salary:
₹4.9 to ₹9.3 Lakhs Per Annum

Qualifications:

  • B.Pharm, M.Pharm, Pharm.D, MSc, BSc, Lifesciences
  • 1 to 5 years of experience

Experience Required:

PositionExperience
Data Manager1-3 years
Senior Data Manager3-5 years

Eligibility:
Candidates willing to join within 1 month are eligible to apply.

How to Apply:
Email your resumes to: ps.shinde@tcs.com
Subject Line: Mention your name and the role you are applying for.

Locations:

  • Mumbai
  • Pune
  • Bangalore
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Teva Pharmaceuticals Hiring Pharmacovigilance Associate Teva Pharmaceuticals

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Job Posting: Pharmacovigilance Associate II at Teva Pharmaceuticals

About Teva Pharmaceuticals

At Teva Pharmaceuticals, we are committed to making good health more affordable and accessible, helping millions worldwide lead healthier lives. As the world’s leading manufacturer of generic medicines and a producer of numerous products on the World Health Organization’s Essential Medicines List, we reach over 200 million people daily. Join us as we continue to make a difference with new ideas and innovative solutions.

Position Details

  • Position Name: Pharmacovigilance Associate II
  • Organization: Teva Pharmaceuticals
  • Location: Bangalore, India, 560052
  • Salary: ₹17.6 Lakhs per year
  • Experience: 5-6 years
  • Qualification: B.Pharm, M.Pharm, Pharm.D, Lifesciences
Apply Online

Responsibilities

TaskDescription
ComplianceEnsure team activities comply with industry standards, company policies, and SOPs through procedural updates and training.
Strategy DevelopmentParticipate in building strategies for global pre-authorization studies and define and execute Teva standards.
Medical EvaluationPerform medical evaluations and clarifications of clinical trial-related adverse events (AE) including narrative content, queries, coding, expectedness, seriousness, and causality with company summary/medical assessment as applicable.
ConsultationAct as a consultant or Single Point of Contact (SPOC) for case-related activities, maintaining a knowledge repository of process updates and changes in real-time.
Safety ReviewProvide aggregate reviews of safety information, including clinical data, to maintain oversight of Teva’s medicinal products’ safety profile.
Administrative SupportAssist in V-Safe related administrative and procedural activities, ensuring all tasks are performed in compliance with work instructions and GVP modules.
Data AnalysisEnsure quality data analysis for trending and prepare the team for process stabilization.
Regulatory ComplianceFollow internal reporting key performance indicators to ensure regulatory compliance.

Qualifications

RequirementDescription
EducationGraduation/Post-graduation in registered life sciences.
ExperienceMinimum of 5-6 years in Pharmacovigilance in a Biopharmaceutical/CRO industry, including experience in a large international organization.
Special SkillsExperience with pre-marketing studies and clinical trial case processing is an asset. In-depth knowledge of international PV regulations.
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EXL Hiring Medical Underwriting Freshers in Multiple Locations

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EXL Hiring Medical Underwriting Freshers in Multiple Locations

Company Overview:
Exlservice Holdings, Inc. is a global analytics and digital solutions company serving various industries, including insurance, healthcare, banking, financial services, media, and retail.

Position Name:
US Medical Underwriting Fresher

Organization:
EXL

Qualifications:

  • B.Pharm
  • M.Pharm

Experience:
0 Years / Freshers

Salary:
₹25,000 – ₹35,000 / month

Locations:

  • Noida
  • Kochi
  • Bangalore

Job Details:

PositionLocationQualificationShiftOperating ModelAvailability
US Medical Underwriting FresherNoida, Kochi, BangaloreB.Pharm, M.PharmUS ShiftHybridImmediate joiners preferred

Application Process:
Interested candidates are invited to share their resumes. Please send your application to Gaurav.kapahi@exlservice.com with the subject line “Medical Underwriting profile”.

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Indian Institute of Science Internship For Freshers

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About the Company:

Join a leading plant molecular biology laboratory at the Indian Institute of Science, Bangalore. Gain hands-on experience with various molecular biology techniques and work with the model plant Arabidopsis.

Position:

Name: Molecular Biology Internship
Organization: Indian Institute of Science
Location: Bangalore
Qualification: Master’s degree in a relevant subject
Experience: 0 Years / Freshers
Salary: Not disclosed

Key Responsibilities:

  • Molecular Cloning: Perform cloning using restriction base, gateway, and Golden Gate methods.
  • Mutant Generation: Use CRISPR/CAS technology to generate mutants.
  • DNA/RNA Isolation & PCR: Isolate DNA/RNA and perform conventional and real-time PCR.
  • Phenotyping: Conduct phenotyping of mutant plants using various assays and microscopy techniques.
  • Plant Maintenance: Manage and maintain plants in the growth room.
  • Record Keeping: Maintain detailed and accurate records of experiments performed daily.

Eligibility Criteria:

  • Available for a full-time (in-office) internship.
  • Can start the internship between 25th May 2024 and 29th June 2024.
  • Available for a duration of 6 months.
  • Possess relevant skills and interests.
  • Final-year master’s degree students or those who have completed their master’s degree in a relevant subject.
  • Sincere and motivated to work with plants.
  • Women wanting to start/restart their careers are encouraged to apply.
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Application Requirements:

  • Submit your CV along with a letter of motivation explaining why you want to apply for this internship and how it will help shape your future career.

Application Deadline:

30th May 2024

Perks:

  • Certificate
  • Letter of recommendation

How to Apply:

Submit your application, including your CV and a letter of motivation, by 30th May 2024. Ensure your application demonstrates your relevant skills, interests, and motivation for applying to this internship.

Meta Description (19 words):
Intern at IISc Bangalore in plant molecular biology. Freshers apply by 30th May 2024. Gain hands-on experience!

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Patient Safety Monitor at Alcon, Bangalore

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Job Posting: Patient Safety Monitor at Alcon, Bangalore

About the Company:
At Alcon, our mission is to provide innovative vision products that enhance the quality of life by helping people see better. We are dedicated to vision research and eye health.

Position Name:
Patient Safety Monitor

Organization:
Alcon

Qualifications:

  • Graduation in Optometry, Pharmacy, M.Pharm, B.Pharm, BDS, BAMS, BHMS

Experience:

  • 1 to 2 Years

Salary:

  • ₹35,000 – ₹55,000 per month

Location:

  • Bangalore
Apply Online

Responsibilities:

Major AccountabilitiesDetails
Case ProcessingProcess case files as per SOPs, coordinate with affiliates, reassess data, and assign codes
ReportingComplete initial and follow-up reports, respond to QA requests, and schedule regulatory reports
ComplianceEnsure adherence to local and international regulations and corporate compliance guidelines
Knowledge MaintenanceMaintain knowledge of Alcon products, anatomy, diseases, procedures, and safety databases
Complaint RecordsProcess and review complaint records for Surgical – Intra Ocular Lens (IOL) as per SOPs
Audits and ReconciliationSupport reconciliation activities and audits
Safety EvaluationEvaluate and escalate potential safety issues to management

Key Performance Indicators:

  • Meeting internal and external quality standards
  • Timely review and closure of files
  • High-quality regulatory report submissions on or before due dates

Ideal Background:

CriteriaDetails
EducationMinimum: Graduation in Science. Desirable: Optometry, Pharmacy, M.Pharm, B.Pharm, BDS, BAMS, BHMS, Biomedical Engineering, or Registered Nurse
ExperienceMinimum: 1-2 years as a healthcare professional. Desirable: Experience in Device Vigilance, Pharmacovigilance, Regulatory Submissions, Clinical Research, PVPI, or Medical Coding

How to Apply:
If you are a dedicated professional ready to enhance patient safety in vision care, please share your CV with us.

Send your CV to: careers@alcon.com

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Medical Editor at Annalect India, Bengaluru

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Job Posting: Medical Editor at Annalect India, Bengaluru

About the Company:
Annalect India, part of Annalect Global and the Omnicom Group, offers premier services in Creative Services, Technology, Marketing Science (data & analytics), and Media Services. Join us and be part of a rapidly growing team delivering top-notch solutions for global clients.

Position Name:
Medical Editor

Organization:
Annalect

Qualifications:

  • B.Pharm, BSc

Experience:

  • 1 to 2 Years

Salary:

  • ₹25,000 – ₹35,000 per month

Location:

  • Bengaluru, Karnataka, India

Responsibilities:

Apply Online
TaskDetails
Copyediting ContentFor pharmaceutical advertising, in-house agencies, or medical publishing.
Adherence to StandardsEnsuring compliance with AMA Manual of Style, 11th edition, grammar, and usage standards.
Software ProficiencyUsing Adobe Acrobat for copyediting tasks.
Team CollaborationWorking with creative teams to ensure high-quality outputs.

How to Apply:
If you are a talented Medical Copy Editor ready to translate creative ideas into impactful designs, please share your CV with us.

Send your CV to: careers@annalect.com

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