"IQVIA Hiring Marketed Product Safety Specialist I | Pharmacovigilance Jobs in Mumbai, Thane, Noida & Chennai 2026"

( IQVIA Hiring Marketed Product Safety Specialist I )

Introduction

If you are looking to start or strengthen your career in pharmacovigilance and drug safety, IQVIA has announced an excellent opportunity for early-career life science professionals. The company is hiring Marketed Product Safety Specialist I across multiple locations in India, including Mumbai, Thane, Noida, and Chennai.

This role is ideal for candidates who want hands-on exposure to lifecycle safety management, pharmacovigilance safety agreements, and global compliance processes while working with one of the world’s most trusted healthcare research organizations.

About The Company – IQVIA 

IQVIA is a globally recognized leader in clinical research services, healthcare intelligence, and pharmacovigilance solutions. The company was formed in 2016 through the merger of IMS Health and Quintiles.

Headquarters: Durham, North Carolina, USA
Global Presence: 100+ countries
Employees: 80,000+ worldwide

IQVIA supports pharmaceutical, biotech, and medical device companies throughout the entire product lifecycle, from clinical development to post-marketing safety and real-world evidence. Its strong focus on data, compliance, and patient safety makes it a preferred employer in the pharma and CRO industry.

Job Overview Summary 

The Marketed Product Safety Specialist I role at IQVIA focuses on post-marketing pharmacovigilance activities, particularly around safety agreements, PSMF documentation, and lifecycle safety support.

This is an entry-level / early-career position where candidates will work under supervision while gaining exposure to global safety operations, client interactions, and regulatory documentation.

Vacancy Details (Official)

• Job Title: Marketed Product Safety Specialist I

• Job ID: R1522371

• Company: IQVIA

• Employment Type: Full-time

• Experience Level: Entry-level / Early career

• Job Locations:

  • Mumbai

  • Thane

  • Noida

  • Chennai

• Last Date to Apply: 22 January 2026

Responsibility Explanation

Selected candidates will be involved in core pharmacovigilance and lifecycle safety operations, including:

• Assisting in drafting and maintaining pharmacovigilance safety agreements

• Supporting safety agreement preparation, review, finalization, and distribution

• Coordinating with internal project teams to define safety responsibilities

• Preparing and updating PSMF (Pharmacovigilance System Master File) documents

• Maintaining safety agreement databases and controlled documentation

• Acting as a secondary customer interface for small safety projects

• Providing operational support to ongoing pharmacovigilance programs

• Ensuring accuracy, compliance, and timely updates of safety records

This role builds a strong foundation for careers in drug safety, PV operations, regulatory compliance, and lifecycle management.

Eligibility Criteria (Official)

Educational Qualification

• Associate’s Degree in Life Sciences, Business Management, or related discipline

• Equivalent education, training, or experience will also be considered

Experience

• Entry-level / early-career professionals

• Basic understanding of pharmacovigilance or lifecycle safety preferred

Skills Required

To succeed in this role, candidates should have:

• Basic to good understanding of pharmacovigilance workflows

• Knowledge of lifecycle safety concepts

• Strong documentation and attention to detail

• Excellent written and verbal English communication

• Ability to manage multiple tasks and deadlines

• Strong organizational and time-management skills

• Team collaboration and stakeholder coordination abilities

Salary Estimate 

Estimated Salary Range:
₹4.5 LPA – ₹7.5 LPA

The final compensation will depend on location, experience, and project assignment, aligned with IQVIA’s internal compensation structure.

Interview Details (Official)

• Interview Mode: Online / Virtual (initial rounds)

• Selection Process:

  • Resume shortlisting

  • Technical & functional interview

  • HR discussion

Only shortlisted candidates will be contacted by IQVIA’s recruitment team.

Required Documents

Candidates should keep the following documents ready:

• Updated resume (ATS-friendly preferred)

• Educational certificates

• Government ID proof

• Experience or internship certificates (if available)

Job Location & Work Environment

📍 Available Locations:
Mumbai | Thane | Noida | Chennai

Candidates may be assigned projects based on business needs and location preference.

How to Apply

Interested and eligible candidates can apply through the official IQVIA career portal:

🔗 Apply Here:
https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Marketed-Prod-Safety-Spec-1_R1522371

FAQs – Marketed Product Safety Specialist IQVIA

Q1. Is this role suitable for freshers?

This role is suitable for entry-level or early-career candidates with basic pharmacovigilance knowledge.

Q2. Is prior PV experience mandatory?

No, but a basic understanding of lifecycle safety and documentation is preferred.

Q3. What type of PV work is involved?

The role mainly focuses on post-marketing safety agreements and lifecycle safety support.

Q4. Is this a permanent position?

Yes, this is a full-time permanent role at IQVIA.

Q5. Does Pharma Duniya charge for job information?

No. Pharma Duniya never charges candidates for job information.

Final Conclusion

The Marketed Product Safety Specialist I role at IQVIA is an excellent entry point for professionals aiming to build a long-term career in pharmacovigilance and global drug safety operations. With exposure to safety agreements, PSMF documentation, and international compliance standards, this opportunity provides both learning and growth within a world-class CRO environment.

Note: Pharma Duniya does not charge any money for job information.
Candidates are advised to verify details from the official company website.

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