Medical Surveillance Associate
Job Description:
๐ ๐๐ถ๐ฟ๐ถ๐ป๐ด: Medical Surveillance Associate | Clinical Research Jobs
๐ ๐๐ผ๐ฐ๐ฎ๐๐ถ๐ผ๐ป: Bangalore, Thane, Pune, Kolkata
๐ผ ๐๐
๐ฝ๐ฒ๐ฟ๐ถ๐ฒ๐ป๐ฐ๐ฒ: 0โ2 Years
๐งพ ๐๐ผ๐ฏ ๐ง๐๐ฝ๐ฒ: Full-Time
๐ข ๐ช๐ผ๐ฟ๐ธ ๐ ๐ผ๐ฑ๐ฒ: Hybrid (3 Days Office + 2 Days Remote)
๐ข ๐๐ผ๐บ๐ฝ๐ฎ๐ป๐: IQVIA
๐ ๐ช๐ฒ๐ฏ๐๐ถ๐๐ฒ: https://www.iqvia.com
๐งพ ๐ฅ๐ผ๐น๐ฒ ๐ข๐๐ฒ๐ฟ๐๐ถ๐ฒ๐:
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.
๐ ๏ธ ๐๐ฒ๐ ๐ฆ๐ธ๐ถ๐น๐น๐:
โ Clinical research and pharmacovigilance knowledge
โ Ability to interpret laboratory and clinical safety data
โ Understanding of medical review and drug safety processes
โ Knowledge of ICSR and clinical trial safety monitoring
โ Strong communication and stakeholder coordination skills
โ Problem-solving abilities for clinical data and reporting issues
โ Knowledge of regulatory compliance and protocol adherence
๐ฏ ๐๐ฒ๐ ๐ฅ๐ฒ๐๐ฝ๐ผ๐ป๐๐ถ๐ฏ๐ถ๐น๐ถ๐๐ถ๐ฒ๐:
โ Monitor clinical laboratory data and identify safety trends
โ Prepare medical narratives and safety summaries
โ Support clinical study safety monitoring activities
โ Coordinate with investigator sites and clinical teams
โ Deliver project-specific operational support and quality control
โ Support SOP development and clinical project setup
โ Represent the Medical Surveillance Team in project meetings
โ Troubleshoot laboratory reporting and data access issues
โ Ensure compliance with protocol and regulatory requirements
โ Maintain updated knowledge through medical journals and training programs
๐ ๐ฅ๐ฒ๐พ๐๐ถ๐ฟ๐ฒ๐ฑ ๐ค๐๐ฎ๐น๐ถ๐ณ๐ถ๐ฐ๐ฎ๐๐ถ๐ผ๐ป๐:
โ BDS / MDS
โ BHMS / BAMS
โ Pharm D / M.Pharm
โ MSc (Life Sciences, Biochemistry, Biotechnology, Microbiology)
โ Candidates with clinical research or pharmacovigilance knowledge preferred
๐ฐ ๐ฆ๐ฎ๐น๐ฎ๐ฟ๐ & ๐๐ฒ๐ป๐ฒ๐ณ๐ถ๐๐:
โ Estimated Salary: โน4 LPA โ โน8 LPA
โ Hybrid work flexibility
โ Exposure to global clinical trials and safety operations
โ Career growth in Pharmacovigilance and Medical Surveillance
โ Opportunity to work with a global healthcare intelligence leader
๐ ๐๐ฏ๐ผ๐๐ ๐๐ค๐ฉ๐๐:
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.
๐ฉ ๐๐ผ๐ ๐๐ผ ๐๐ฝ๐ฝ๐น๐:
Send your updated resume to:
๐ง priyanka.ganapavarapu@iqvia.com
๐ง pavan.cm@iqvia.com
๐ฌ ๐๐ผ๐ถ๐ป ๐ช๐ต๐ฎ๐๐๐๐ฝ๐ฝ ๐๐ฟ๐ผ๐๐ฝ:
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