FSP Clinical Scientist – Clinical Development
Company: Syneos Health
Location: Gurugram, India
Job ID: 25104707
Job Type: Full-time | Functional Service Provider (FSP) Model
Experience Required: 3–8 years (preferred)
Date Updated: January 9, 2026
Job Overview
Syneos Health, a global biopharmaceutical solutions organization, is seeking an experienced FSP Clinical Scientist to support early- and late-phase clinical development programs. This role partners closely with Medical Directors and cross-functional teams to ensure scientific integrity, data quality, and regulatory compliance throughout the clinical trial lifecycle.
The position is based in Gurugram, India, and operates within a Functional Service Provider (FSP) environment, offering exposure to global clinical trials and innovative development models.
About Syneos Health
Syneos Health is a fully integrated biopharmaceutical services organization operating across 110+ countries with over 29,000 professionals worldwide. The company has supported 94% of Novel FDA-approved drugs and 95% of EMA-authorized products in the last five years.
At Syneos Health, innovation, agility, and patient-centric development drive everything we do.
Key Responsibilities
Collaborate with the Medical Director to develop and execute medical plans, including:
Medical Management Plans
Medical Data Review Plans
Eligibility Review Plans
Conduct regular and ad-hoc medical reviews of clinical data listings and visualizations to identify trends, safety signals, and data risks.
Author, review, and manage medical data queries; assess responses and approve query closure in coordination with Medical Directors.
Support patient profile reviews, protocol deviation assessments, and preparation of Medical Review Summary Reports as required.
Participate in medical data review meetings and safety review meetings, including preparation of scientific presentations and slides.
Act as a key interface between internal stakeholders, sponsors, and vendors for medical data and eligibility review activities.
Collaborate with Clinical Operations, Data Management, Pharmacovigilance, Drug Safety, and Project Management teams to ensure subject safety and data integrity.
Identify and escalate project risks, timeline deviations, and out-of-scope activities in a timely manner.
Participate in Trusted Process meetings and contribute to internal and external audits.
Maintain working knowledge of protocol designs, disease areas, and relevant medical terminology.
Ensure compliance with ICH-GCP guidelines, data privacy regulations, SOPs, work instructions, and sponsor-specific requirements.
Required Qualifications
Advanced degree in Life Sciences such as MSc, PharmD, PhD, MD, DMD, or equivalent.
3–8 years of relevant experience in clinical research, clinical development, medical review, or related pharmaceutical roles (experience range may vary based on qualifications).
Strong understanding of ICH-GCP guidelines, clinical trial processes, and drug development lifecycle.
Demonstrated ability to analyze clinical data and apply scientific judgment to ensure data quality and patient safety.
Excellent written and verbal communication skills in English.
Proficiency in MS Office applications (Word, Excel, PowerPoint).
Strong organizational skills with the ability to manage multiple priorities in a regulated and fast-paced environment.
Proven ability to work independently as well as collaboratively in cross-functional global teams.
Why Join Syneos Health
Global exposure to high-impact clinical development programs
Structured career development and progression opportunities
Supportive leadership and continuous learning culture
Competitive total rewards and recognition programs
Inclusive and diverse work environment promoting innovation and collaboration
Equal Opportunity Statement
Syneos Health is an equal opportunity employer committed to diversity, inclusion, and compliance with global employment laws. Reasonable accommodations are provided in accordance with applicable regulations. Equivalent education and experience may be considered.
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