Job Title: FSP Clinical Scientist
Company: Syneos Health
Location: Gurugram, India
Job ID: 25104707
Updated: January 9, 2026
Company Overview:
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating drug development and improving patient outcomes. With a presence in over 110 countries and 29,000 employees worldwide, Syneos Health combines clinical, medical affairs, and commercial expertise to deliver innovative solutions tailored to modern healthcare challenges.
Position Summary:
Syneos Health is seeking an experienced FSP Clinical Scientist to provide clinical and scientific input across early- and late-stage clinical development programs. This role emphasizes protocol-specific requirements, scientific integrity, and data quality in clinical trials. The Clinical Scientist will collaborate closely with Medical Directors and cross-functional teams to conduct medical data reviews, support regulatory compliance, and ensure high-quality execution of clinical studies.
This position is ideal for candidates with a strong scientific background, experience in clinical trials, and proficiency in data analysis within a regulated pharmaceutical environment.
Key Responsibilities:
Medical and Clinical Oversight
Collaborate with Medical Directors to develop medical plans including Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan.
Engage external experts, consultants, and advisors to acquire scientific input for medical plans.
Conduct regular and ad-hoc medical review of clinical trial data, identifying risks, trends, and patterns to support medical documentation.
Author medical data queries, review responses, and approve query closure in collaboration with the Medical Director.
Assist in reviewing patient profiles, protocol deviations, and other study-level data as needed.
Prepare slides and reports for medical data review and safety meetings.
Project Management and Collaboration
Manage project scope, objectives, and quality of deliverables to meet study-specific timelines.
Serve as primary interface between internal teams, clients, and vendors for medical data and eligibility review.
Collaborate with Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, and Project Management to identify risks related to data integrity and subject safety.
Escalate study concerns, out-of-scope tasks, and project risks to leadership in a timely manner.
Participate in Trusted Process meetings, internal audits, and external audits as required.
Regulatory Compliance and Scientific Excellence
Acquire knowledge of protocol designs, disease terminology, and pathology relevant to clinical studies.
Adhere to ICH-GCP guidelines, data privacy regulations, enterprise policies, SOPs, and project plans.
Ensure high-quality medical data analysis through rigorous scientific assessment and attention to detail.
Qualifications:
Education:
Advanced degree in Life Sciences (MSc, PharmD, PhD, DMD, MD) or equivalent.
Experience:
Relevant scientific experience in clinical research, drug development, or clinical operations.
Familiarity with ICH-GCP guidelines and regulatory compliance in clinical trials.
Proven ability to handle multiple tasks, meet deadlines, and deliver high-quality work in a dynamic environment.
Strong analytical, problem-solving, and decision-making skills.
Technical & Professional Skills:
Excellent written and verbal communication skills.
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
Ability to collaborate effectively within cross-functional teams.
Self-starter with flexibility to adapt to changing priorities and timelines.
Understanding of scientific principles and clinical trial data analysis.
Why Join Syneos Health?
Contribute to cutting-edge clinical research and innovative drug development.
Work in a global, collaborative environment with diverse teams.
Access professional development opportunities and mentorship from industry leaders.
Join a culture that values inclusion, innovation, and excellence in patient care.
Apply Now:
This is an exceptional opportunity for clinical scientists to advance their career while making an impact on global patient safety and clinical research excellence.
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