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