Associate Clinical Project Management Director, Cross TA

Role responsibilities

The Associate Clinical Project Management Director will lead and coordinate global and regional clinical trial management activities, ensuring successful planning, execution, and closure of trials. They will act as a primary contact for stakeholders and oversee trial deliverables while maintaining compliance and quality.

Requirements

Candidates must have a bachelor's degree in Life Sciences and a minimum of 8 years of experience in clinical trials, with proven leadership in complex trials. Strong knowledge of ICH-GCP and local regulatory requirements is essential, along with excellent communication and analytical skills.

Key skills

Clinical Trial Management, Leadership, Communication, Decision-Making, Analytical Skills, Regulatory Compliance, Budget Planning, Vendor Coordination, Training Development, Project Management, Stakeholder Engagement, Inspection Readiness, Data Management, Monitoring, Problem Solving, Team Coordination

Keywords

Clinical Trials, Trial Management, Study Management Team, Inspection Readiness, Regulatory Submissions, Health Authority Inspections, Budget Monitoring, Out-of-Pocket Costs, FTE Cost Drivers, Monitoring Guidelines, Informed Consent Forms, Blinding Plans, Central Trial Activities, Enrollment Commitments, Vendor Management, Clinical Systems, CTMS, TMF, IVRS, Central Labs, ePRO, Imaging, Translation, Ancillary Supplies, CAPA Processes, Investigator Meetings, Training Materials, Feasibility Assessments, Recruitment Plans, Trial Documentation