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Fsp Clinical Scientist

Syneos Health
Syneos Health
2-5 years
Not Disclosed
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

FSP Clinical Scientist
Location: Gurugram, India | Job ID: 25104707 | Employment Type: Full-Time

About Syneos Health
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization, dedicated to accelerating customer success and improving patient outcomes worldwide. By integrating clinical, medical affairs, and commercial insights, we deliver innovative solutions that address the evolving challenges of drug development and healthcare delivery.

Our Clinical Development model places the patient and customer at the center of all activities. At Syneos Health, we simplify processes, streamline workflows, and foster an environment that makes us both easy to work with and a rewarding workplace.

Role Overview
The FSP Clinical Scientist partners with Medical Directors to provide clinical and scientific expertise across early- and late-stage clinical development programs. The role ensures scientific integrity, data quality, and compliance with regulatory and clinical standards while supporting medical plan development, data review, and risk assessment.

Key Responsibilities

  • Collaborate with Medical Directors to develop medical plans, including Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans.

  • Engage external experts, consultants, and advisors to ensure accurate and comprehensive medical/scientific input.

  • Perform regular and ad-hoc medical data reviews, analyzing trends, identifying risks, and supporting documentation.

  • Author and review medical queries, oversee query closure, and contribute to Medical Review Summary reports.

  • Prepare slides and support safety review meetings and medical data review sessions.

  • Manage project scope, objectives, and quality deliverables to meet timelines and milestones.

  • Collaborate cross-functionally with Clinical Operations, Data Management, Drug Safety/Pharmacovigilance, and Project Management teams.

  • Escalate study concerns, including risks to subject safety or data integrity, to project leads promptly.

  • Participate in Trusted Process meetings, audits, and internal or external regulatory inspections.

  • Maintain knowledge of protocol designs, disease terminology, pathology, and applicable ICH/GCP guidelines.

Required Qualifications & Experience

  • Degree in Life Sciences (MSc, PharmD, PhD, DMD, MD) or equivalent.

  • Minimum 2–5 years of relevant experience in clinical development, medical review, or drug development.

  • Proficient in medical data analysis, scientific documentation, and protocol evaluation.

  • Strong understanding of ICH/GCP guidelines, clinical trial processes, and regulatory requirements.

  • Excellent time management, communication, and interpersonal skills.

  • Proficiency in MS Office, including spreadsheets and presentations.

  • Ability to work independently, adapt to changing priorities, and escalate issues appropriately.

  • Demonstrated ability to collaborate effectively in a cross-functional, multinational team environment.

Why Syneos Health

  • Access to global career development and therapeutic area training.

  • Supportive culture promoting diversity, inclusion, and professional growth.

  • Exposure to innovative clinical trials across multiple therapeutic areas, impacting patient outcomes worldwide.

  • Opportunity to work in a collaborative environment with a global network of experts.

Equal Employment Opportunity
Syneos Health is an equal opportunity employer committed to diversity, inclusion, and compliance with local and international employment laws. Reasonable accommodations are available for qualified individuals during the recruitment process.

Apply Now
Join Syneos Health as an FSP Clinical Scientist to advance your career in clinical research, medical data review, and drug development while contributing to meaningful patient outcomes globally.