Location: Gurugram / Hyderabad, India (Hybrid)
Company: Syneos Health
Job ID: 25107044
Experience Required: 3–6 years (Not suitable for freshers)
About the Company
Syneos Health is a globally recognized, fully integrated biopharmaceutical solutions organization focused on accelerating customer success. With deep expertise across the clinical development and commercialization lifecycle, the company partners with innovators to deliver impactful healthcare solutions worldwide.
Job Overview
The Senior Medical Scientist plays a critical role in supporting early and late-phase clinical development programs. This position involves close collaboration with Medical Directors and cross-functional teams to ensure scientific integrity, regulatory compliance, and high-quality clinical trial execution.
Key Responsibilities
Collaborate with Medical Directors to develop comprehensive medical plans including Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan
Conduct ongoing and ad-hoc medical data reviews, identifying trends, risks, and inconsistencies in clinical datasets
Generate, review, and resolve medical data queries in alignment with study protocols
Support scientific review activities including patient profiles, protocol deviations, and study-level data analysis
Contribute to medical review meetings, safety discussions, and presentation development
Ensure timely delivery of project milestones while maintaining data quality and compliance standards
Act as a key interface between internal teams, sponsors, and external stakeholders
Work closely with Clinical Operations, Data Management, Pharmacovigilance, and Project Management teams
Participate in audits, compliance checks, and internal review processes
Maintain adherence to ICH-GCP guidelines, SOPs, and global regulatory standards
Required Qualifications
Advanced degree in Life Sciences, Pharmacy, or Medicine (MD, PharmD, PhD preferred)
3–6 years of relevant experience in clinical research, medical review, or drug development
Strong understanding of clinical trial processes, data review, and medical monitoring
Familiarity with ICH-GCP, regulatory guidelines, and clinical data systems
Excellent analytical, communication, and stakeholder management skills
Why Consider This Role
Opportunity to work on global clinical trials across therapeutic areas
Exposure to high-impact drug development programs
Collaborative and innovation-driven work environment
Strong career progression pathways within a global CRO ecosystem
Important Note for Applicants
This role requires prior experience in clinical research or medical review. Freshers are encouraged to explore entry-level roles such as Clinical Research Associate (CRA), Drug Safety Associate, or Medical Writer positions before applying to senior-level opportunities like this.
How to Apply
Visit the official company careers page or apply through trusted job portals. For more verified global pharma jobs, visit ThePharmaDaily.com
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