FSP Clinical Scientist – Pune, Hybrid
Location: Pune, India (Hybrid)
Employment Type: Full-Time
Job ID: 25104707
Experience Required: 3+ Years
Industry: Biopharmaceuticals | Clinical Research | Functional Service Provider (FSP)
About Syneos Health
Syneos Health® is a global, fully integrated biopharmaceutical solutions organization dedicated to accelerating clinical development and commercial success. By combining deep expertise in clinical operations, medical affairs, and data analytics, we deliver solutions that ensure high-quality clinical trials and improved patient outcomes.
With over 29,000 employees across 110+ countries, we foster a collaborative, innovative, and patient-focused environment, supporting both Functional Service Provider (FSP) partnerships and full-service solutions.
Role Overview
We are seeking a highly skilled FSP Clinical Scientist to provide scientific and clinical expertise for hematology-focused clinical trials, with anticipated indications in myeloma or lymphoma. The role primarily focuses on scientific data review, supporting medical plans, and collaborating with cross-functional teams to ensure the accuracy, integrity, and quality of clinical trial data.
The Clinical Scientist will work closely with Medical Directors, project teams, and external experts to deliver high-quality medical and scientific outputs while adhering to regulatory and GCP standards.
Key Responsibilities
Conduct comprehensive medical and scientific data reviews for hematology clinical trials, including patient profiles, adverse events, concomitant medications, efficacy and safety data, and PD analyses
Support Lead Scientist and Medical Directors in the preparation of Medical Management Plans, Medical Data Review Plans, and Eligibility Review Plans
Collaborate with external consultants and advisors to obtain necessary medical/scientific input for protocol-specific plans
Author and review medical data queries, ensuring timely resolution and proper documentation
Participate in medical data review meetings, safety reviews, and slide preparation for internal and external presentations
Analyze clinical data to identify risks, trends, and patterns, providing actionable insights to project teams
Serve as a liaison between internal teams, vendors, and clients, ensuring smooth project execution and timely deliverables
Support internal and external audits and Trusted Process meetings as required
Maintain compliance with ICH, GCP, data privacy guidelines, SOPs, and project-specific plans
Mentor junior clinical staff and provide guidance on data review processes, as needed
Required Qualifications
Degree in Life Sciences (MSc, PharmD, PhD, DMD, MD) or equivalent with relevant scientific or clinical experience
3+ years of experience in clinical trial data review or clinical science within oncology, hematology, or related therapeutic areas
Proficiency in clinical data analysis, medical query management, and report preparation
Strong knowledge of ICH/GCP guidelines, drug development processes, and clinical trial protocols
Excellent written and verbal communication skills and ability to collaborate in cross-functional teams
High proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and clinical data systems
Strong time management, problem-solving, and organizational skills to handle multiple tasks in a dynamic environment
Self-starter with ability to adapt to changing timelines, priorities, and project scopes
Why Join Syneos Health
Contribute to global clinical programs impacting FDA- and EMA-approved products
Work with a diverse, high-performing team in a collaborative, innovative environment
Professional growth opportunities with mentorship and cross-functional exposure
Access to industry-leading clinical systems, processes, and expertise
Inclusive workplace fostering diversity, equity, and authenticity
Equal Opportunity Statement
Syneos Health is an equal opportunity employer. We consider qualified applicants without regard to race, gender, disability, or background. Transferable skills and equivalent experience may be considered. Reasonable accommodations will be provided in compliance with applicable law.
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