Sr Medical Scientist — Syneos Health
Job Overview
A clinical and scientific role supporting medical oversight of clinical trials, focusing on data review, medical input, and collaboration with clinical development teams to ensure study integrity and patient safety.
Location: Gurugram, India (Hybrid)
Job ID: 25107054
Job Family: Clinical / Medical Science
Employment Type: Full-time
Role Purpose
To partner with Medical Directors in providing scientific and clinical oversight across clinical trials, ensuring:
Data quality and integrity
Patient safety
Protocol compliance
Scientific validity of study outputs
Key Responsibilities
1. Medical & Scientific Support
Work with Medical Directors to develop:
Medical Management Plans
Medical Data Review Plans
Eligibility Review Plans
Gather scientific input from experts and advisors
2. Clinical Data Review
Perform regular and ad-hoc medical review of clinical trial data
Analyze data listings and visualizations to identify:
Safety signals
Trends and risks
Document findings from medical reviews
3. Query & Data Management
Write and manage medical data queries
Review responses and approve query closures with Medical Director
Support patient profile reviews and protocol deviation assessments
Assist in medical review summary reports
4. Cross-functional Collaboration
Work closely with:
Clinical Operations
Data Management
Pharmacovigilance / Drug Safety
Project Management
Lead or participate in study meetings and data review discussions
Identify and escalate risks related to safety or data integrity
5. Study Execution Support
Ensure study milestones and timelines are met
Serve as interface between internal teams, clients, and vendors
Support preparation of presentations for review meetings
6. Compliance & Quality
Ensure adherence to:
ICH guidelines
GCP (Good Clinical Practice)
Data privacy regulations
Company SOPs and protocols
Participate in audits and inspections when required
Required Qualifications
Education
Life sciences / medical / pharmacy background (implied requirement)
Experience
Experience in clinical research or clinical development preferred
Understanding of:
Clinical trial design
Medical terminology
Disease areas and pathology
Skills
Strong analytical and scientific reasoning skills
Ability to interpret clinical data trends
Good communication and documentation skills
Ability to work in cross-functional teams
Attention to detail and regulatory awareness
Key Competencies
Clinical data interpretation
Medical review and risk identification
Cross-functional collaboration
Regulatory compliance (ICH-GCP)
Scientific writing and documentation
Career Level
Mid-level scientific/clinical contributor role
May involve limited team supervision responsibilities
Job Impact
Ensures clinical trial scientific integrity
Supports patient safety monitoring
Helps improve accuracy of clinical study outcomes
Acts as a bridge between medical, data, and operations teams
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