Associate Clinical Project Manager

Job Title:
Associate Clinical Project Manager

Department:
Clinical Operations / Global Clinical Sciences

Overview:

Seeking an
Associate Clinical Project Manager (ACPM)
to support the successful execution of global clinical trials from protocol through study closeout.

Key Responsibilities:

Study & Documentation Management

• Maintain Trial Master File (TMF) in an inspection-ready state
• Support development and review of study documents (protocols, ICFs, CSRs, study plans)
• Assist with clinical data review to ensure quality and completeness
• Support contract, budget, and invoice tracking activities

Project Coordination & Communication

• Coordinate communication across internal teams, vendors, and CROs
• Track study timelines, metrics, and status updates
• Support and document study team meetings and action items
• Assist with vendor and site coordination

Quality & Compliance

• Support audit and inspection readiness activities
• Assist with issue resolution and quality improvement initiatives
• Ensure compliance with GCP and regulatory requirements

Training & Systems Support

• Assist with development and tracking of study-specific training
• Support investigator meetings and study start-up activities
• Provide support for CTMS and other clinical systems

Qualifications:

• Bachelor’s degree required
• 1–2 years of CRA or clinical research experience
• Understanding of clinical trial phases (Phase I–IV)
• Strong organizational, communication, and problem-solving skills