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Fsp Clinical Scientist

Syneos Health
Syneos Health
0-2 years
Not Disclosed
10 Jan. 19, 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 – Gurugram, India

Location: Gurugram, India
Job Type: Full-Time
Job ID: 25104707

About Syneos Health

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization, delivering innovative solutions across clinical development, medical affairs, and commercial operations. With a presence in 110 countries and over 29,000 employees, we leverage scientific expertise, advanced technology, and operational excellence to accelerate clinical programs and ensure high-quality patient outcomes.

Our mission is to simplify and optimize clinical operations, placing the patient and customer at the center of every decision while fostering a collaborative and growth-oriented work environment.

Position Overview

The FSP Clinical Scientist will partner with Medical Directors to provide clinical and scientific input across early and late-stage clinical development programs. This role emphasizes protocol-specific requirements, ensuring scientific integrity and high-quality data throughout clinical trials. The position requires collaboration with cross-functional teams to support data review, safety monitoring, and clinical decision-making.

This role is ideal for professionals with a strong life sciences background, experience in clinical trial execution, and the ability to analyze and interpret clinical data to guide operational and scientific strategies.

Key Responsibilities

  • Partner with Medical Directors to develop Medical Management Plans, including Medical Data Review Plans and Eligibility Review Plans.

  • Engage with external experts and consultants to acquire medical/scientific input for clinical projects.

  • Conduct regular and ad-hoc medical reviews of clinical data listings, visualizations, and analyses to identify trends, risks, or safety signals.

  • Author medical data queries, review responses, and approve query closure in coordination with Medical Directors.

  • Assist in patient profile reviews, scientific assessments of study-level data, protocol deviation analysis, and creation of Medical Review Summary Reports.

  • Support medical data review meetings and safety review meetings, including slide preparation and presentations.

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

  • Serve as primary interface with internal teams, clients, and vendors for medical data review and eligibility assessments.

  • Collaborate with Clinical Operations, Data Management, Pharmacovigilance, and Project Management teams to ensure data integrity and subject safety.

  • Participate in Trusted Process meetings, internal and external audits as required.

  • Maintain knowledge of protocol designs, disease terminology, and pathology relevant to assigned studies.

  • Adhere to GCP, ICH, and data privacy standards, as well as enterprise policies, SOPs, and client requirements.

Required Qualifications

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

  • Proven ability to manage multiple tasks and meet deadlines in a regulated, dynamic environment.

  • Strong understanding of clinical trial principles, scientific data analysis, and regulatory guidelines (ICH/GCP).

  • Excellent written and verbal communication skills.

  • Proficiency in MS Office (Word, Excel, PowerPoint).

  • Self-starter capable of handling fluctuating timelines, shifting priorities, and escalations.

  • Strong team collaboration and cross-functional interpersonal skills.

Why Join Syneos Health?

  • Contribute to cutting-edge clinical development programs supporting novel therapies.

  • Collaborate with global teams across multiple disciplines in a dynamic, growth-focused environment.

  • Opportunity to ensure scientific integrity and patient safety in clinical trials.

  • Be part of a company committed to diversity, inclusion, and professional development.

Apply now to join Syneos Health as an FSP Clinical Scientist and advance your career in clinical research and scientific oversight.