Unlock senior pharmacovigilance jobs at IQVIA with the Associate Medical Safety Director role in Bengaluru. Hybrid pharma jobs offering medical expertise in drug safety. Explore clinical research careers in India today.
Contents
About the Company
IQVIA stands as a global powerhouse in the life sciences sector, delivering advanced analytics, technology solutions, and clinical research services to accelerate innovative treatments worldwide.
Founded through the merger of IMS Health and Quintiles, the NYSE-listed firm (IQV) combines data science with human insights to drive healthcare progress, serving pharmaceutical manufacturers and beyond with unmatched regulatory compliance and real-world evidence expertise.
Its expansive global footprint spans over 100 countries, fostering sustainable growth and empowering professionals in pharmaceutical careers in India through cutting-edge pharmacovigilance and safety monitoring innovations.
Job Details
- Company Name: IQVIA
- Experience: 3 years clinical practice + 2 years in pharmaceutical industry (or equivalent)
- Qualification: Medical degree from accredited international medical school; valid medical license preferred
- Location: Bengaluru, India (also available in Ahmedabad)
- Work Type: Hybrid
Job Description
IQVIA is actively recruiting for the Associate Medical Safety Director to bolster its pharmacovigilance services, providing expert oversight on trials and safety projects.
This senior role demands a blend of clinical acumen and regulatory savvy to ensure patient safety across global portfolios. Ideal for seasoned professionals seeking impactful pharmacovigilance jobs in clinical research.
Associate Medical Safety Director
- Department: Medical Safety / Pharmacovigilance
- Role: Deliver medical expertise on adverse events, safety reviews, and regulatory reports for trials and post-marketing
- Experience: 3 years clinical + 2 years pharma (or equivalent)
- Education/Qualification: Medical degree; valid license preferred
Skills/Qualifications
- In-depth knowledge of federal and local regulations for clinical research and pharmacovigilance
- Expertise in good clinical practice (GCP), safety reporting, and causality assessment
- Proficiency in clinical trials processes and pharmaceutical research methodologies
- Strong analytical skills for reviewing AEs, ADRs, and aggregate safety data
- Excellent communication for client consultations and cross-functional collaboration
- Ability to manage priorities, deadlines, and multiple assignments effectively
- Initiative, flexibility, and relationship-building with stakeholders
Key Responsibilities
- Review and clarify AEs/ADRs for narrative, coding, and causality
- Compose and edit Analyses of Similar Events (AOSE) per regulations
- Consult on case processing and aggregate safety profile oversight
- Vet coding for medical histories and concomitant medications
- Present safety findings in client and project meetings
- Edit IND reports, PSURs, and risk management plans
- Oversee label development and Data Safety Monitoring Boards
- Review protocols, IDBs, and CRFs for safety content
- Provide 24-hour medical support and escalation as needed
Benefits/Perks
- Accelerated career growth with global mobility and leadership programs
- Extensive learning via pharmacovigilance certifications and training
- Competitive salary with performance incentives and bonuses
- Inclusive hybrid work culture promoting innovation and balance
- Broad global exposure through international projects and collaborations
- Comprehensive health, wellness, and retirement benefits
How to Apply
To apply for this Associate Medical Safety Director position, visit https://jobs.iqvia.com and search for job code R1497935. Submit your resume, cover letter, and credentials directly through the portal. Tailor your application to highlight pharmacovigilance expertise for faster review.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the IQVIA Career page.
For more pharmacovigilance jobs and career advice in pharmaceutical careers in India, check Pharma Recruiter. Apply now—shape the future of drug safety at IQVIA!
Why You Should Join
IQVIA fosters a culture of excellence and recognition, celebrating contributions to patient outcomes through awards, mentorship, and collaborative innovation hubs. Experience unmatched career stability in a resilient global leader navigating regulatory complexities with agility.
Seize abundant growth opportunities, from specialized PV training to executive tracks, in an environment blending cutting-edge tech with ethical compliance—empowering you to drive real-world healthcare advancements daily.
FAQs
What qualifications are required for Associate Medical Safety Director at IQVIA?
A medical degree from an accredited school is essential, plus 3 years clinical experience and 2 years in pharma. A valid medical license is preferred for pharmacovigilance jobs.
How do I apply for these clinical research jobs in Bengaluru?
Search for R1497935 on https://jobs.iqvia.com and submit your application online. Highlight relevant safety review experience for hybrid pharma roles.
What growth paths exist in IQVIA’s pharmacovigilance team?
Roles evolve to senior director levels with global projects and certifications. Visit Pharma Recruiter for insights on advancement in India.
Is hybrid work flexible for pharmaceutical careers at IQVIA?
Yes, Bengaluru (and Ahmedabad) positions offer hybrid setups, balancing office collaboration with remote efficiency in a supportive environment.