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Fsp Clinical Scientist

Syneos Health
Syneos Health
3-5 years
preferred by company
10 Feb. 5, 2026
Job Description
Job Type: Full Time 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

FSP Clinical Scientist

Updated: February 3, 2026
Location: Gurgaon, Haryana, India
Job ID: 25104707
Employment Type: Full-Time | Functional Service Provider (FSP)


About Syneos Health

Syneos Health® is a leading global biopharmaceutical solutions organization dedicated to accelerating customer success. By integrating clinical development, medical affairs, and commercial expertise, Syneos Health delivers patient-centric, data-driven solutions that address the evolving demands of global healthcare.

With over 29,000 professionals across 110 countries, Syneos Health partners with customers to advance innovative therapies and improve patient outcomes worldwide.


Role Overview

The FSP Clinical Scientist partners closely with Medical Directors and cross-functional clinical teams to provide scientific and medical expertise across early- and late-phase clinical development programs. This role focuses on high-quality scientific data review, medical data analysis, and ensuring the integrity, safety, and regulatory compliance of clinical trials, with a primary emphasis on hematology indications such as multiple myeloma and lymphoma.


Key Responsibilities

Scientific & Medical Data Review

  • Perform comprehensive medical and scientific data review for hematology clinical trials, including anticipated indications in myeloma and lymphoma.

  • Review standard clinical data listings, including adverse events, concomitant medications, laboratory data, and other safety datasets.

  • Conduct patient profile reviews, efficacy evaluations, safety narrative reviews, pharmacodynamic (PD) analyses, and PD data reviews as required.

  • Support the Lead Clinical Scientist in scientific review activities across assigned clinical studies.

Medical Management & Collaboration

  • Collaborate with Medical Directors to develop and maintain key medical plans, including the Medical Management Plan, Medical Data Review Plan, and Eligibility Review Plan.

  • Engage with external experts, consultants, and advisors to obtain medical and scientific input supporting clinical trial execution.

  • Participate in medical data review and safety review meetings, including preparation of scientific presentations and review materials.

Data Analysis & Quality Oversight

  • Perform routine and ad-hoc medical reviews of data listings and data visualizations to identify safety risks, data trends, and potential issues.

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

  • Assist with protocol deviation reviews, Medical Review Summary reports, and other study-level scientific documentation as needed.

Project & Stakeholder Management

  • Manage assigned scope of work, deliverables, and timelines to ensure project milestones are met with high quality standards.

  • Serve as a key interface between internal teams, sponsors, and vendors for medical data and eligibility review activities.

  • Collaborate with Clinical Operations, Data Management, Biostatistics, Drug Safety/Pharmacovigilance, and Project Management teams to proactively identify and escalate risks related to data integrity and patient safety.

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

Compliance & Continuous Learning

  • Maintain a working understanding of protocol designs, disease areas, and relevant clinical terminology and pathology.

  • Ensure adherence to data privacy requirements, ICH guidelines, Good Clinical Practice (GCP), company SOPs, work instructions, and sponsor-specific procedures.


Required Qualifications

Education

  • Master’s or Doctoral degree in Life Sciences (MSc, PharmD, PhD, MD, DMD) or equivalent scientific discipline

Experience

  • Minimum 3–5 years of relevant experience in clinical research, clinical science, medical review, or related roles within the pharmaceutical, biotechnology, or CRO industry

  • Experience supporting clinical trials in hematology or oncology is preferred

Skills & Competencies

  • Strong understanding of clinical development processes and scientific principles

  • Working knowledge of ICH, GCP, and regulatory requirements governing clinical trials

  • Excellent analytical, problem-solving, and data interpretation skills

  • Strong written and verbal communication abilities

  • Proficiency in Microsoft Office applications, including Word, Excel, and PowerPoint

  • Ability to manage multiple priorities in a fast-paced, highly regulated environment

  • Proven ability to work independently and collaboratively within cross-functional teams


Why Join Syneos Health

  • Work on high-impact global clinical development programs

  • Collaborate with industry-leading scientific and medical professionals

  • Access structured career development, technical training, and therapeutic area learning

  • Be part of a diverse, inclusive, and patient-focused global organization

Over the past five years, Syneos Health has contributed to:

  • 94% of all novel FDA-approved drugs

  • 95% of EMA-authorized products

  • More than 200 studies across 73,000 sites and over 675,000 clinical trial participants


Additional Information

This job description is not exhaustive and may be adjusted based on business needs. Syneos Health is an equal opportunity employer and complies with all applicable employment and accessibility regulations. Reasonable accommodations will be provided as required by law.


Job Summary

The FSP Clinical Scientist provides scientific and clinical expertise to support early- and late-stage clinical development programs. Working closely with Medical Directors and cross-functional teams, this role ensures the scientific integrity, data quality, and compliant execution of clinical trials through rigorous medical data review and medical management activities.