FSP Clinical Scientist – Hematology Clinical Trials
Job ID: 25104707-OTHLOC-5449-2DH
Employment Type: Full-Time
Work Model: FSP (Functional Service Provider)
Location: Madhapur, Telangana, India
Last Updated: January 22, 2026
Experience Required: 3–6 Years
Therapeutic Area: Hematology (Myeloma / Lymphoma)
Industry: Clinical Research | Biopharmaceuticals | CRO
Job Overview
Syneos Health is seeking a skilled FSP Clinical Scientist to support early- and late-phase hematology clinical trials. This role partners closely with Medical Directors to deliver high-quality medical and scientific data review, ensuring the integrity, safety, and regulatory compliance of clinical trial data.
The Clinical Scientist will play a key role in protocol-driven medical data review, patient safety evaluation, and cross-functional collaboration within a global clinical development environment.
Key Responsibilities
Perform comprehensive medical and scientific data review for hematology clinical trials, with focus on multiple myeloma and lymphoma
Conduct standard clinical data listing reviews, including adverse events, concomitant medications, efficacy data, and safety parameters
Support patient profile reviews, safety narrative reviews, pharmacodynamic analyses, and efficacy assessments as required
Collaborate with Lead Clinical Scientist and Medical Director on study-level medical data review activities
Develop and support Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans in collaboration with Medical Directors
Perform routine and ad-hoc review of data listings and visualizations to identify safety signals, data trends, and potential risks
Author medical data queries, review query responses, and approve query closures in coordination with Medical Director
Support preparation of Medical Review Summary Reports, protocol deviation reviews, and study-level analyses
Participate in medical data review meetings and safety review meetings, including preparation of presentation materials
Act as primary interface for medical data review activities across internal teams, sponsors, and vendors
Collaborate with Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, and Project Management teams to identify and escalate risks to data integrity or subject safety
Ensure adherence to ICH-GCP guidelines, data privacy regulations, enterprise SOPs, and sponsor-specific requirements
Support audit readiness activities and participate in internal and external audits as required
Maintain foundational knowledge of protocol design, disease biology, and therapeutic area terminology
Required Qualifications
Advanced degree in Life Sciences or Medicine (MSc, PharmD, PhD, MD, DMD, or equivalent)
Minimum 3 years of relevant experience in clinical research, clinical science, or medical data review
Solid understanding of clinical trial data, safety reporting, and scientific principles applicable to drug development
Working knowledge of ICH-GCP guidelines and global clinical research regulations
Strong analytical skills with ability to identify safety risks, trends, and data inconsistencies
Excellent written and verbal communication skills in English
Proficiency in Microsoft Office applications, including Word, Excel, and PowerPoint
Ability to manage multiple priorities in a fast-paced, highly regulated environment
Strong collaboration skills and ability to work effectively within cross-functional teams
Preferred Qualifications
Experience supporting hematology or oncology clinical trials
Prior experience in an FSP or CRO environment
Exposure to medical data visualization tools and clinical trial databases
About Syneos Health
Syneos Health is a leading global biopharmaceutical solutions organization, supporting clinical development, medical affairs, and commercial strategies across the product lifecycle. Over the past five years, Syneos Health has contributed to nearly all novel FDA-approved drugs and a majority of EMA-authorized products worldwide.
With operations in more than 110 countries and a workforce of over 29,000 professionals, Syneos Health is committed to accelerating therapies that change lives.
Why This Role Matters
This role offers the opportunity to work at the intersection of science, medicine, and data, contributing directly to the quality and success of global clinical trials in high-impact therapeutic areas.
Gujarat :
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