FSP Clinical Scientist – Hyderabad, Hybrid
Location: Hyderabad, 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, fully integrated biopharmaceutical solutions organization committed to accelerating clinical development and commercial success. Leveraging expertise across clinical operations, medical affairs, pharmacovigilance, and biostatistics, we deliver high-quality solutions that enhance patient outcomes and streamline drug development.
With 29,000+ employees across 110+ countries, Syneos Health fosters an innovative, collaborative, and patient-centric environment, supporting both Functional Service Provider (FSP) partnerships and full-service solutions.
Role Overview
We are seeking a highly skilled FSP Clinical Scientist to provide scientific and clinical expertise for hematology-focused clinical trials, primarily in myeloma and lymphoma indications. This role emphasizes scientific data review, collaboration with Medical Directors, and ensuring the accuracy, integrity, and quality of clinical trial outputs.
The Clinical Scientist will contribute to protocol-specific medical plans, analyze trial data, manage queries, and coordinate with cross-functional teams to deliver high-quality clinical insights.
Key Responsibilities
Perform medical and scientific data review for hematology clinical trials, including adverse events, concomitant medications, efficacy data, and patient profiles
Support Lead Scientist and Medical Directors with Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans
Author, review, and approve medical queries, ensuring timely resolution in coordination with the Medical Director
Analyze clinical trial data to identify risks, trends, and safety signals, supporting documentation and reporting of findings
Collaborate with study teams including Clinical Operations, Data Management, Pharmacovigilance, and Project Management to ensure data integrity and subject safety
Participate in medical review meetings, safety review meetings, and Trusted Process meetings; support audit processes as required
Provide input to medical review summaries and support protocol deviation assessments
Adhere to ICH, GCP, data privacy guidelines, SOPs, work instructions, and customer-specific policies
Mentor junior clinical staff and support development of best practices in scientific data review and medical management
Required Qualifications
Degree in Life Sciences (MSc, PharmD, PhD, DMD, MD) or equivalent with relevant clinical or scientific experience
3+ years of experience in clinical data review, medical/scientific data analysis, or clinical operations
Strong knowledge of ICH/GCP guidelines, clinical trial protocols, and oncology/hematology therapeutic areas
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and clinical data systems
Excellent written and verbal communication skills with strong attention to detail
Ability to prioritize multiple tasks, work independently, and thrive in a dynamic, high-pressure environment
Strong interpersonal skills with a collaborative approach to working in cross-functional teams
Why Join Syneos Health
Work on global clinical programs impacting FDA- and EMA-approved products
Collaborate with cross-functional teams in an innovative, patient-focused environment
Gain exposure to advanced clinical systems, medical plans, and regulatory processes
Access professional development, mentorship, and career progression opportunities
Contribute to a diverse, inclusive, and authentic workplace
Equal Opportunity Statement
Syneos Health is an equal opportunity employer. We welcome applicants regardless of race, gender, disability, or background. Transferable skills and equivalent experience may be considered. Reasonable accommodations are provided in compliance with applicable law.
Apply Now
Take the next step in your career with Syneos Health. Apply to become an FSP Clinical Scientist and make a measurable impact on clinical trial outcomes and patient lives globally.
Gujarat :
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Ranchi |Sikkim :
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Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Frank Scottile Blvd |Missouri :
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Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Tallinn |Hà Nội :
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Kyiv |Lima Region :
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Niš |Bohemia :
Prague |Chile :
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