Job Description
*****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...
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...
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