Sr. Clinical Trial Associate

Role: Senior Clinical Trial Associate supporting bipolar mania studies in a biopharma setting, focused on trial document management, compliance, and coordination. Responsibilities: maintain inspection-ready TMF per ICH-GCP, track and support study documentation, vendor invoices, and contract activities, assist with study communication materials, and support trial logistics and ad-hoc activities. Requirements: Bachelor's in life sciences or healthcare, 3+ years in clinical trial support, preferably in biotech/pharma; strong computer skills (Excel, Word, PowerPoint, Outlook); understanding of clinical trial operations; ability to multitask independently in a fast-paced environment; proactive team player. HighValue: support for bipolar disorder clinical trials, trial document oversight, vendor and contract management, with a focus on GCP compliance. WorkSetup: hybrid Boston, onsite Mon-Wed; collaborative, innovative environment.