Senior Clinical Trial Associate

The Sr Clinical Trial Associate (Sr CTA) position will assist with daily clinical trial execution activities including the coordination of documents associated with the conduct of investigational clinical studies in accordance with applicable regulations, Good Clinical Practice (GCP), and Synthekine standard operating procedures (SOPs). The Sr CTA will support the Associate Director, Clinical Trials in day-to-day activities for managing clinical trial conduct. The ideal candidate will have keen attention to detail and the ability both to prioritize and handle multiple tasks effectively in a rapidly growing company environment. The role reports to the Associate Director, Clinical Trials. Responsibilities include organizing/maintaining tracking systems for clinical studies, collecting and disseminating trial information, scheduling and coordinating study meetings, updating and maintaining eTMF, training coordination, managing version control of clinical documents, communicating effectively with team members, liaising with contract organizations, tracking clinical trial supplies, and supporting various project tasks.