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Fsp Clinical Scientist

Syneos Health
Syneos Health
3-6 years
preferred by company
10 Feb. 4, 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 – Hematology (Myeloma & Lymphoma)

Updated: Yesterday
Location: Pune, Maharashtra, India
Job ID: 25104707-OTHLOC-5580-2DR


Job Overview

Syneos Health® is a globally recognized, fully integrated biopharmaceutical solutions organization supporting the development and delivery of innovative therapies across the clinical lifecycle. By combining clinical development, medical affairs, and commercial expertise, Syneos Health enables sponsors to accelerate timelines while maintaining the highest scientific and regulatory standards.

We are seeking an experienced FSP Clinical Scientist to support hematology clinical trials, with a primary focus on myeloma and lymphoma indications. This role is aligned to a Functional Service Provider (FSP) model and will focus predominantly on scientific and medical data review activities in collaboration with Medical Directors and cross-functional study teams.


Experience Required

  • 3–6 years of experience in clinical research or clinical science roles within pharmaceutical, biotechnology, or CRO environments

  • Hands-on experience supporting hematology clinical trials (myeloma, lymphoma, or related oncology indications preferred)

  • Demonstrated experience in medical and scientific data review for clinical studies

  • Working knowledge of ICH-GCP guidelines and clinical trial processes


Key Responsibilities

Scientific & Medical Data Review

  • Perform detailed medical and scientific data review for hematology clinical trials

  • Conduct standard data listing reviews, including adverse events, concomitant medications, and laboratory data

  • Review patient profiles, efficacy and safety data, pharmacodynamic (PD) analyses, and safety narratives

  • Support the Lead Clinical Scientist with ongoing scientific data review activities

Medical Management Support

  • Collaborate with the Medical Director to develop and support Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans

  • Draft medical data queries, review query responses, and approve query closure in collaboration with the Medical Director

  • Assist with protocol deviation reviews, medical review summaries, and study-level scientific assessments as required

Cross-Functional Collaboration

  • Partner with Clinical Operations, Data Management, Pharmacovigilance, Drug Safety, and Project Management teams to identify and mitigate risks related to data integrity and subject safety

  • Support medical data review and safety review meetings, including preparation of presentation materials

  • Serve as a primary interface for medical data review activities across internal teams, sponsors, and vendors

Project & Compliance Oversight

  • Manage assigned scope of work to ensure project milestones, timelines, and quality expectations are met

  • Escalate data quality issues, safety concerns, and out-of-scope activities to project leadership in a timely manner

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

  • Ensure compliance with ICH, GCP, data privacy regulations, SOPs, and client-specific procedures


Qualifications & Skills

Education

  • Advanced degree in Life Sciences such as MSc, PharmD, PhD, MD, or equivalent

  • Relevant scientific or clinical training will be considered

Core Competencies

  • Strong understanding of clinical trial design, disease pathology, and scientific data interpretation

  • Excellent written and verbal communication skills in English

  • Strong organizational and time-management skills with the ability to manage multiple priorities

  • Proficiency in Microsoft Office applications (Word, Excel, PowerPoint)

  • Ability to work independently and effectively within cross-functional, global teams

  • Proven problem-solving skills with appropriate escalation judgment


Why Join Syneos Health

  • Opportunity to support programs contributing to 94% of novel FDA-approved drugs and 95% of EMA-authorized products

  • Exposure to global hematology and oncology clinical development programs

  • Structured career development, scientific training, and mentoring

  • Inclusive, collaborative culture that values scientific excellence and diversity


About Syneos Health

Over the past five years, Syneos Health has supported more than 200 clinical studies across 73,000 sites and 675,000+ trial patients worldwide. With a workforce of 29,000+ professionals across 110 countries, Syneos Health continues to drive innovation in clinical research and medical development.


Disclaimer

The responsibilities outlined above are not exhaustive and may evolve based on project needs. Syneos Health reserves the right to determine equivalent qualifications and experience. This posting does not constitute an employment contract. The company is committed to equal employment opportunity and compliance with applicable employment and accessibility regulations.