Medical Surveillance Associate

IQVIA
๐Ÿ‘œ 0 - 2 years
๐Ÿ“ Bangalore, Thane, Pune, Kolkata
๐Ÿ’ผ Hybrid
๐Ÿ’ฐ Not Disclosed
Posted on May 07, 2026

Job Description:

๐Ÿš€ ๐—›๐—ถ๐—ฟ๐—ถ๐—ป๐—ด: Medical Surveillance Associate | Clinical Research Jobs 
๐Ÿ“ ๐—Ÿ๐—ผ๐—ฐ๐—ฎ๐˜๐—ถ๐—ผ๐—ป: Bangalore, Thane, Pune, Kolkata 
๐Ÿ’ผ ๐—˜๐˜…๐—ฝ๐—ฒ๐—ฟ๐—ถ๐—ฒ๐—ป๐—ฐ๐—ฒ: 0โ€“2 Years 
๐Ÿงพ ๐—๐—ผ๐—ฏ ๐—ง๐˜†๐—ฝ๐—ฒ: Full-Time 
๐Ÿข ๐—ช๐—ผ๐—ฟ๐—ธ ๐— ๐—ผ๐—ฑ๐—ฒ: Hybrid (3 Days Office + 2 Days Remote) 
๐Ÿข ๐—–๐—ผ๐—บ๐—ฝ๐—ฎ๐—ป๐˜†: IQVIA 
๐ŸŒ ๐—ช๐—ฒ๐—ฏ๐˜€๐—ถ๐˜๐—ฒ: https://www.iqvia.com ;

๐Ÿงพ ๐—ฅ๐—ผ๐—น๐—ฒ ๐—ข๐˜ƒ๐—ฒ๐—ฟ๐˜ƒ๐—ถ๐—ฒ๐˜„:
IQVIA India is actively hiring Medical Surveillance Associates for multiple locations across India. This is an excellent opportunity for candidates interested in clinical research, pharmacovigilance, medical monitoring, and clinical safety operations.

The role focuses on medical surveillance support, clinical laboratory data monitoring, safety reporting, and collaboration with global clinical teams to ensure patient safety and protocol compliance during clinical trials.

This opportunity is ideal for candidates from Pharmacy, Life Sciences, Healthcare, and Medical backgrounds who want to build a long-term career in drug safety, clinical operations, and medical review domains.

๐Ÿ› ๏ธ ๐—ž๐—ฒ๐˜† ๐—ฆ๐—ธ๐—ถ๐—น๐—น๐˜€:
โœ” Clinical research and pharmacovigilance knowledge 
โœ” Ability to interpret laboratory and clinical safety data 
โœ” Understanding of medical review and drug safety processes 
โœ” Knowledge of ICSR and clinical trial safety monitoring 
โœ” Strong communication and stakeholder coordination skills 
โœ” Problem-solving abilities for clinical data and reporting issues 
โœ” Knowledge of regulatory compliance and protocol adherence 

๐ŸŽฏ ๐—ž๐—ฒ๐˜† ๐—ฅ๐—ฒ๐˜€๐—ฝ๐—ผ๐—ป๐˜€๐—ถ๐—ฏ๐—ถ๐—น๐—ถ๐˜๐—ถ๐—ฒ๐˜€:
โœ” Monitor clinical laboratory data and identify safety trends 
โœ” Prepare medical narratives and safety summaries 
โœ” Support clinical study safety monitoring activities 
โœ” Coordinate with investigator sites and clinical teams 
โœ” Deliver project-specific operational support and quality control 
โœ” Support SOP development and clinical project setup 
โœ” Represent the Medical Surveillance Team in project meetings 
โœ” Troubleshoot laboratory reporting and data access issues 
โœ” Ensure compliance with protocol and regulatory requirements 
โœ” Maintain updated knowledge through medical journals and training programs 

๐ŸŽ“ ๐—ฅ๐—ฒ๐—พ๐˜‚๐—ถ๐—ฟ๐—ฒ๐—ฑ ๐—ค๐˜‚๐—ฎ๐—น๐—ถ๐—ณ๐—ถ๐—ฐ๐—ฎ๐˜๐—ถ๐—ผ๐—ป๐˜€:
โœ” BDS / MDS 
โœ” BHMS / BAMS 
โœ” Pharm D / M.Pharm 
โœ” MSc (Life Sciences, Biochemistry, Biotechnology, Microbiology) 
โœ” Candidates with clinical research or pharmacovigilance knowledge preferred 

๐Ÿ’ฐ ๐—ฆ๐—ฎ๐—น๐—ฎ๐—ฟ๐˜† & ๐—•๐—ฒ๐—ป๐—ฒ๐—ณ๐—ถ๐˜๐˜€:
โœ” Estimated Salary: โ‚น4 LPA โ€“ โ‚น8 LPA 
โœ” Hybrid work flexibility 
โœ” Exposure to global clinical trials and safety operations 
โœ” Career growth in Pharmacovigilance and Medical Surveillance 
โœ” Opportunity to work with a global healthcare intelligence leader 

๐ŸŒŸ ๐—”๐—ฏ๐—ผ๐˜‚๐˜ ๐—œ๐—ค๐—ฉ๐—œ๐—”:
IQVIA is a global leader in clinical research services, healthcare intelligence, and advanced analytics. The company supports pharmaceutical and healthcare organizations in accelerating drug development and improving patient outcomes worldwide.

๐Ÿ“ฉ ๐—›๐—ผ๐˜„ ๐˜๐—ผ ๐—”๐—ฝ๐—ฝ๐—น๐˜†:
Send your updated resume to: 
๐Ÿ“ง priyanka.ganapavarapu@iqvia.com 
๐Ÿ“ง pavan.cm@iqvia.com 

๐Ÿ’ฌ ๐—๐—ผ๐—ถ๐—ป ๐—ช๐—ต๐—ฎ๐˜๐˜€๐—”๐—ฝ๐—ฝ ๐—š๐—ฟ๐—ผ๐˜‚๐—ฝ:
๐Ÿ‘‰ Join now

Required Skills:

Problem-solving abilities for clinical data and reporting issues, Knowledge of regulatory compliance and protocol adherence
โœ” Verified