FSP Clinical Scientist – Hematology
Updated: Yesterday
Location: Gurgaon, Haryana, India
Job ID: 25104707-OTHLOC-5206-2DH
Employment Type: Full-Time | Functional Service Provider (FSP)
About Syneos Health®
Syneos Health® is a leading fully integrated biopharmaceutical solutions organization dedicated to accelerating customer success. By combining clinical development, medical affairs, and commercial expertise, Syneos Health delivers end-to-end solutions that address evolving global healthcare and regulatory challenges.
With a presence across 110+ countries and a patient-centric Clinical Development model, Syneos Health partners with sponsors through both Functional Service Provider (FSP) and Full-Service models to advance innovative therapies worldwide.
Position Overview
The FSP Clinical Scientist provides scientific and medical data review support for global hematology clinical trials, with a primary focus on indications such as multiple myeloma and lymphoma. This role partners closely with the Medical Director and cross-functional study teams to ensure high-quality scientific data review, protocol compliance, subject safety, and regulatory adherence across early- and late-phase clinical studies.
The position is primarily focused on scientific data review, with additional clinical scientist responsibilities as required by project scope.
Key Responsibilities
Scientific and Medical Data Review
Perform medical and scientific data review for hematology clinical trials, including safety, efficacy, and pharmacodynamic (PD) data
Conduct standard data listing reviews, including adverse events, concomitant medications, and patient profiles
Review safety narratives, efficacy outputs, PD analyses, and data visualizations to identify trends, risks, and data anomalies
Author medical data queries, review responses, and approve query closure in collaboration with the Medical Director
Clinical Trial Support and Collaboration
Support the Lead Clinical Scientist and Medical Director with protocol-specific scientific reviews and study-level analyses
Assist in patient profile review, protocol deviation review, and preparation of Medical Review Summary reports as needed
Participate in medical data review meetings and safety review meetings, including slide preparation and documentation
Collaborate with Clinical Operations, Data Management, Drug Safety, Pharmacovigilance, and Project Management teams to ensure data integrity and subject safety
Medical Management and Compliance
Contribute to the development of Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans
Ensure compliance with ICH-GCP, data privacy regulations, enterprise SOPs, work instructions, and customer-specific procedures
Participate in Trusted Process meetings and internal or external audits as required
Maintain foundational knowledge of protocol designs, disease pathology, and therapeutic area terminology
Required Qualifications and Experience
Education
Advanced degree in Life Sciences such as MSc, PharmD, PhD, MD, or equivalent with relevant scientific or clinical research experience
Experience
2–5 years of experience in clinical research, clinical science, medical review, or related roles within the pharmaceutical, biotechnology, or CRO industry
Prior experience supporting hematology clinical trials (multiple myeloma, lymphoma preferred) is highly desirable
Exposure to early- and/or late-phase clinical development programs
Skills and Competencies
Strong understanding of clinical trial data, safety review, and scientific analysis
Working knowledge of drug development processes and ICH-GCP guidelines
Excellent written and verbal communication skills
Strong analytical, organizational, and time management abilities
Proficiency in Microsoft Office applications (Word, Excel, PowerPoint)
Ability to work independently and collaboratively in a fast-paced, regulated environment
Proactive mindset with the ability to escalate issues appropriately
Why Join Syneos Health?
Opportunity to work on high-impact global hematology trials
Collaborative, inclusive, and scientifically driven work culture
Ongoing career development, therapeutic training, and mentoring
Exposure to innovative clinical development programs across multiple regions
Over the past five years, Syneos Health has supported:
94% of novel FDA-approved drugs
95% of EMA-authorized products
200+ studies across 73,000 sites and 675,000+ clinical trial participants
Additional Information
Job responsibilities may evolve based on project and business needs
Equivalent education and experience combinations will be considered
This job description does not constitute an employment contract
Syneos Health is an equal opportunity employer and complies with all applicable employment and accessibility regulations
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