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Fsp Clinical Scientist

Syneos Health
Syneos Health
3-7 years
preferred by company
10 Jan. 19, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ 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

Job Title: FSP Clinical Scientist
Location: Gurgaon, Haryana, India (Hybrid)
Employment Type: Full-Time
Experience Required: 3–7 years in Clinical Science / Medical Data Review / Clinical Operations
Job ID: 25104707
Updated: January 9, 2026


Job Overview

Syneos Health®, a global leader in biopharmaceutical solutions, is seeking an experienced FSP Clinical Scientist to join our Clinical Development team. This role partners closely with Medical Directors to provide scientific and clinical expertise, ensuring data quality, protocol compliance, and the integrity of clinical trials across early and late-stage development programs.

The FSP Clinical Scientist will support medical management, data review, and eligibility assessments, collaborating with cross-functional teams including Clinical Operations, Data Management, Drug Safety, and Pharmacovigilance. This role is ideal for a proactive professional with strong analytical skills, attention to detail, and the ability to manage multiple priorities in a dynamic, highly regulated environment.


Key Responsibilities

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

  • Engage with external experts, consultants, and advisors to acquire scientific input required for medical plan development.

  • Conduct regular and ad-hoc medical review of study data, including data listings, visualizations, and identification of trends or risks.

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

  • Assist in patient profile reviews, protocol deviation analyses, and preparation of Medical Review Summary reports.

  • Participate in medical data review and safety review meetings; prepare presentation materials and summaries as needed.

  • Manage project scope, milestones, and quality of deliverables; serve as primary interface between internal teams, customers, and vendors for medical data and eligibility review activities.

  • Collaborate with cross-functional teams to identify risks related to data integrity and patient safety; escalate issues and out-of-scope tasks as appropriate.

  • Attend internal Trusted Process meetings and participate in audits as required.

  • Ensure adherence to data privacy guidelines, ICH standards, GCP, SOPs, and client-specific procedures.


Required Qualifications

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

  • 3–7 years of experience in clinical data review, medical management, or clinical operations in pharmaceutical or CRO settings.

  • Solid understanding of clinical trial processes, study protocols, and medical data analysis.

  • Knowledge of ICH/GCP guidelines, drug development processes, and clinical safety requirements.

  • Strong analytical and problem-solving skills with attention to detail.

  • Excellent written and verbal communication skills.

  • Proficiency in MS Office (Word, Excel, PowerPoint) and ability to produce clear, high-quality documentation.

  • Ability to work independently and collaboratively in a cross-functional team environment.


Why Join Syneos Health?

  • Work on global clinical trials supporting FDA-approved and EMA-authorized drugs.

  • Opportunity to collaborate with a team of passionate professionals across Medical Affairs, Safety, and Clinical Operations.

  • Engage in career development, training programs, and leadership growth opportunities.

  • Be part of an inclusive and diverse culture, where innovation and scientific excellence are recognized and rewarded.


Apply now on ThePharmaDaily.com to advance your career as an FSP Clinical Scientist with a leading global biopharmaceutical organization.