Clinical Scientist
TScan Therapeutics·GV (Consider)
Waltham, MAClinical Scientist$145k–$155kPosted Jul 1, 2026
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Clinical Scientist
Department:
30 - Clinical
Location:
Waltham, MA
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Position Summary:
TScan is seeking a highly motivated and detail-oriented Clinical Scientist with deep expertise in clinical data management and data review to support the execution of our oncology cell therapy clinical programs. This unique role sits at the intersection of Clinical Development, Clinical Operations, Data Management, and Biostatistics serving as a critical driver of data quality, data integrity, and clinical insight generation.
The Clinical Scientist will be responsible for leading ongoing clinical data review activities, developing data review strategies, identifying and resolving data issues, and ensuring high-quality clinical datasets are available to support safety reviews, regulatory submissions, and clinical decision-making. The successful candidate will possess a strong scientific background combined with hands-on experience in clinical data management, EDC systems, data visualization tools, and cross-functional collaboration.
This position offers an opportunity to play a highly visible role in advancing innovative TCR-T therapies through clinical development while helping establish best-in-class data review and clinical science processes.
Key Responsibilities
Clinical Data Review & Oversight
Serve as the clinical lead for ongoing data review activities across TScan clinical studies.
Develop and execute comprehensive data review plans to ensure timely identification and resolution of data discrepancies, trends, and potential safety signals.
Review patient-level clinical data to assess completeness, consistency, protocol compliance, and medical relevance.
Partner with Clinical Operations, Data Management, Medical, Pharmacovigilance, and Biostatistics to drive data quality and readiness.
Lead cross-functional data review meetings and track resolution of key data issues.
Clinical Science & Data Interpretation
Analyze and interpret emerging clinical, safety, efficacy, and biomarker data to support study conduct and decision-making.
Support data cleaning efforts for interim analyses, data monitoring committee reviews, and regulatory submissions.
Contribute to clinical narratives, safety analyses, data listings review, and study reports.
Collaborate with translational and biomarker teams to integrate clinical and correlative data insights.
Data Management Collaboration
Partner closely with Data Management to review CRFs, edit checks, data validation plans, and data review specifications.
Provide clinical input into database design, study builds, and data collection strategies.
Support UAT testing of EDC systems and associated clinical technologies.
Review data transfer specifications and external vendor data integration processes.
Ensure data review activities align with CDISC standards and regulatory expectations.
Clinical Development Support
Contribute to protocol development, endpoint definitions, and data collection strategies.
Participate in study team meetings and provide clinical science expertise throughout study execution.
Support preparation of clinical study reports (CSRs), regulatory documents, investigator brochures, and publications.
Assist with inspection and audit readiness activities.
Process Improvement & Innovation
Develop and implement innovative approaches for ongoing clinical data surveillance and risk-based data review.
Leverage data visualization tools and analytics platforms to enhance clinical data review efficiency.
Contribute to the development of clinical data review SOPs, work instructions, and best practices.
Help establish scalable...