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.
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