This role involves owning key operational aspects of clinical trials, including TMF integrity and vendor coordination, while also mentoring junior team members. The Senior Clinical Trial Associate will independently manage the study TMF plan from development to archiving, lead quality reviews, resolve discrepancies with CROs, and draft study documents with minimal oversight. They will also serve as a resource for junior CTAs, manage clinical supply and lab sample coordination, handle data reconciliation issues, represent Clinical Operations in meetings, and contribute to training materials and SOPs.
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Job Type
Full-time
Career Level
Senior