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Lead Protocol Design & Authorship: Oversee Phase I–III oncology trials, including feasibility, pilot, and pivotal studies. Translate scientific hypotheses into operationally- and submission-ready protocols, develop study synopses, and lead protocol amendments. Endpoint & Population Selection: Select appropriate endpoints, patient populations, and clinical instruments, while developing robust scientific justifications for your selections. Documentation Development:...
About the Role
Clinical Trial Protocol Specialist
Our client an innovative medical device startup are currently recruiting for a Clinical Trial Protocol Specialist to join their team on a permanent basis. As Clinical Trial Protocol Specialist you will lead the design and authorship of investigational protocols across their expanding portfolio. You will work at the intersection of clinical science, regulatory strategy, and study operations.
Responsibilities
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