FSP Clinical Scientist – Remote, India
Location: Remote, India
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 leading global biopharmaceutical solutions organization focused on accelerating clinical development and improving patient outcomes. We deliver integrated solutions spanning clinical operations, medical affairs, pharmacovigilance, biostatistics, and scientific communications, enabling efficient and compliant drug development.
Our Clinical Development model places patients and customers at the center of every decision. By simplifying workflows and fostering cross-functional collaboration, we create an environment where innovation thrives and therapies reach patients faster.
Role Overview
We are seeking a FSP Clinical Scientist to provide scientific and clinical expertise for hematology clinical trials, primarily in myeloma and lymphoma indications. The role focuses on medical data review, patient profile assessments, efficacy and safety analyses, and supporting Medical Directors in Medical Management Plans and trial-specific deliverables.
This is a remote role in India, with collaboration across global teams, ensuring the quality, integrity, and regulatory compliance of clinical trial data.
Key Responsibilities
Conduct scientific and medical data reviews for hematology clinical trials, including adverse events, concomitant medications, patient profiles, and efficacy assessments
Support Lead Scientist and Medical Directors in Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans
Analyze trial data to identify risks, patterns, and trends, documenting findings for regulatory and internal review
Author, review, and approve medical data queries in coordination with Medical Directors
Partner with study teams including Clinical Operations, Data Management, Pharmacovigilance, and Project Management to ensure data integrity and patient safety
Support medical review meetings, safety review meetings, and audit processes
Provide guidance on protocol deviations, Medical Review Summaries, and scientific assessments
Maintain compliance with ICH, GCP, data privacy guidelines, SOPs, and project plans
Mentor junior clinical staff and contribute to cross-functional training and process improvements
Required Qualifications
Degree in Life Sciences (MSc, PharmD, PhD, DMD, MD) or equivalent
3+ years of experience in clinical data review, medical/scientific analysis, or clinical operations
Strong knowledge of ICH/GCP guidelines and clinical trial protocols
Experience with hematology, oncology, or related 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 and attention to detail
Ability to work independently and in cross-functional global teams
Why Join Syneos Health
Engage with global clinical programs impacting FDA- and EMA-approved products
Collaborate with cross-functional teams on innovative drug development projects
Contribute to regulatory-compliant, high-quality clinical trial outputs
Access career development, training, and mentorship opportunities
Work in a diverse, inclusive, and collaborative workplace that values innovation and ownership
Equal Opportunity Statement
Syneos Health is an equal opportunity employer. We encourage 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 today to join as an FSP Clinical Scientist and contribute to global clinical trials that advance patient care.
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