Amgen Hiring Senior Associate Medical Data Reviewer

Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what’s known today.

Post : Senior Associate Medical Data Reviewer

Job Description
In this vital role, the Senior Associate - Medical Data Reviewer is responsible for ensuring the clinical integrity, quality, and interpretability of data generated across the clinical development lifecycle. The role applies strong medical and scientific judgment to complex clinical datasets to safeguard patient safety, enable timely signal detection, and support regulatory-ready decision making. The position requires both clinical expertise and analytical rigor, with the ability to distinguish clinically meaningful signals from background variability and drive appropriate actions when required.

• Conduct ongoing medical review of clinical trial data to ensure accuracy, consistency, and clinical relevance.
• Evaluate adverse events, laboratory data, vital signs, ECGs, imaging, and other key safety and efficacy endpoints.
• Identify trends, outliers, protocol deviations, and emerging safety signals across studies.
• Apply medical judgment to distinguish clinically meaningful findings from normal variability.
• Provide medical input into study start-up activities, including risk assessments and data review strategy.
• Partner cross-functionally with Clinical Operations, Data Management, Safety, Biostatistics, and vendors to resolve data issues.
• Contribute to the development and refinement of medical review tools, visualizations, and dashboards (e.g., Spotfire).
• Lead or contribute to data review meetings, governance discussions, and issue escalation processes.
• Author and maintain clear, defensible medical documentation to support inspection readiness.
• Drive continuous improvement by identifying systemic data quality trends and strengthening review standards and workflows.

Candidate Profile
• MBBS, MD, PharmD, BDS, BAMS, BHMS, or other relevant medical/healthcare degree with clinical research experience
OR
• Master’s degree in Life Sciences, Pharmacy, Public Health, or related field with 5+ years of clinical research experience
OR
• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related discipline with 7+ years of clinical research experience

Candidate Profile
• 5+ years of experience in clinical research within biotech, pharmaceutical, or CRO environments
• Experience reviewing large, complex clinical trial datasets
• Understanding of clinical data review processes and study conduct within GCP environments
• Experience with clinical data analysis or visualization tools (e.g., Spotfire, Power BI, or similar)
• Ability to interpret complex clinical datasets and translate findings into clear, actionable insights
• Strong written and verbal communication skills with experience presenting to cross-functional and leadership audiences

Additional Information
Experience : 5+ years
Qualification : Degree in Life Sciences, Pharmacy
Location : Hyderabad
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Clinical
End Date : 31st August 2026