*****The position is primarily onsite in Wayne, PA, with an expectation of working in the office two days per week.*****
The Clinical Trial Associate supports the planning, execution, and delivery of clinical trials in alignment with internal standard operating procedures, ICH/GCP guidelines, and applicable regulatory requirements. This role works closely with the Clinical Operations study management team to ensure efficient study management, adherence to timelines and budgets, and consistently high-quality standards. The position is a 6‑month contract with potential conversion to full-time employment.
Responsibilities

+ Create and review study plans, specification documents, study materials, and operational tools to support effective trial conduct.

+ Support outsourced activities to Clinical Research Organizations (CROs) and other third-party vendors for assigned study tasks.

+ Track study progress in the clinical trial management system (CTMS), includ...