FSP Clinical Scientist – Gurugram, Hybrid
Location: Gurugram, India (Hybrid)
Employment Type: Full-Time
Job ID: 25104707
Experience Required: 3+ Years
Industry: Biopharmaceuticals | Clinical Research | Functional Service Provider (FSP)
About Syneos Health
Syneos Health® is a global leader in biopharmaceutical solutions, delivering integrated services across clinical development, medical affairs, pharmacovigilance, and scientific communications. Our mission is to accelerate the delivery of therapies while ensuring patient-centric outcomes.
Our Clinical Development model positions patients and customers at the center of every project. We continuously innovate, simplify workflows, and foster cross-functional collaboration to enhance efficiency, quality, and impact in clinical trials.
Role Overview
We are seeking an experienced FSP Clinical Scientist to provide scientific and clinical expertise for hematology clinical trials, particularly in myeloma and lymphoma indications. This role focuses on medical data review, patient profile assessments, efficacy and safety evaluations, and supporting Medical Directors in Medical Management and trial-specific deliverables.
This hybrid position in Gurugram offers the opportunity to work on high-impact, global clinical trials while collaborating with cross-functional teams across the organization.
Key Responsibilities
Conduct medical and scientific data reviews for hematology clinical trials, including adverse events, concomitant medications, patient profiles, efficacy analyses, and safety narratives
Support Lead Scientist and Medical Directors in developing Medical Management Plans, Data Review Plans, and Eligibility Review Plans
Analyze trial data to identify risks, trends, and patterns, ensuring documentation is accurate and regulatory compliant
Author, review, and approve medical data queries in coordination with Medical Directors
Collaborate with Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, and Project Management teams to maintain data integrity and patient safety
Prepare presentations, summaries, and reports for medical data review and safety meetings
Participate in internal audits, Trusted Process meetings, and cross-functional project discussions
Maintain compliance with ICH, GCP, data privacy regulations, SOPs, and project plans
Mentor junior clinical staff and contribute to training, process improvement, and knowledge sharing
Required Qualifications
Degree in Life Sciences (MSc, PharmD, PhD, DMD, MD) or equivalent
Minimum 3 years of relevant clinical research or medical/scientific data review experience
Strong knowledge of ICH/GCP guidelines and clinical trial protocols
Experience in hematology or oncology therapeutic areas preferred
Excellent analytical, problem-solving, and time management skills
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and clinical data systems
Strong written and verbal communication skills
Ability to work independently and within global, cross-functional teams
Why Join Syneos Health
Contribute to high-impact clinical trials supporting FDA- and EMA-approved products
Work in a diverse, inclusive, and collaborative environment
Access career development, mentorship, and training programs
Drive innovation in clinical trial execution and medical data analysis
Play a key role in ensuring regulatory-compliant, high-quality clinical trial outputs
Equal Opportunity Statement
Syneos Health is an equal opportunity employer. Applicants are encouraged to apply regardless of race, gender, disability, or background. Transferable skills and equivalent experience are considered. Reasonable accommodations are provided in compliance with applicable law.
Apply Now
Join Syneos Health as an FSP Clinical Scientist and contribute your expertise to global clinical trials that advance patient care and therapeutic development.
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