Experteer Overview
In this role you support Oncology Therapeutic programs by assisting the Clinical Study Lead in designing, executing, and evaluating Phase 1–3 studies. You ensure data quality to inform governance and regulatory submissions. You work with Clinical Operations to start up global studies, monitor safety, and oversee data review and reporting. You contribute to regulatory readiness and Investigator/Advisory Board activities, while driving process improvements in the clinical trial delivery model. You will collaborate cross-functionally to shape study conduct in a fast-paced, science-driven environment.

Compensation / Benefits
• Support end-to-end delivery of clinical study protocols including design, initiation, data monitoring, dissemination and closeout
• Collaborate on study start-up to enable on-schedule site activation and enrollment; optimize study parameters to reduce risk and improve site performance
• Participate in inspection readiness activities for audits and regulatory inspections
• Perform and coordinate clinical data review and analysis (CRFs, data listings, coding, patient profiles) to ensure data integrity
• Oversee clinical studies in collaboration with the Clinical Study Lead and external partners; interpret data and ensure timely deliverables
• Support safety decisions with Clinical Safety & Pharmacovigilance in line with the protocol
• Contribute to Investigator Meetings and Advisory Board meeting content
• Author/review regulatory-compliant study documents (protocols, consent, DSURs, IBs, INDs, marketing applications)
• Support evolution of the clinical science role and drive process improvements in the trial delivery model

Tasks
• 8+ years of clinical development experience in pharma/biotech
• Strong oncology knowledge and drug development experience
• Experience ensuring data integrity and performing exploratory analyses; familiarity with clinical data analytics platforms (e.g., Medidata Rave, Elluminate, Spotfire) is preferred
• Excellent written, oral, and presentation skills
• Ability to travel up to 15%
• Location: Cambridge, MA or Princeton, NJ with in-office 70%/30% WFH flexibility
• Experience working in a matrix environment and cross-functional collaboration
• Knowledge of regulatory standards and ability to author regulatory documents

Key requirements
• best-in-class healthcare coverage
• well-being resources (fitness, mindfulness, mental health)
• family planning benefits (fertility, adoption, surrogacy)
• generous paid time off (vacation, volunteer days, sabbatical)
• discretionary year-end shutdown
• savings and investment opportunities