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 key member of the Study Management Team, interfacing with stakeholders to ensure compliance and timely delivery of trial milestones.

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 at a large pharmaceutical company. 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, Budget Planning, Regulatory Compliance, 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, ICH-GCP, Regulatory Requirements, Vendor Management, Budget Oversight, Health Authority Inspections, Training Materials, Investigator Meetings, Out-of-Pocket Costs, FTE Cost Drivers, Monitoring Guidelines, Central Trial Activities, CAPA Processes, Enrollment Commitments, Feasibility Assessments, Inspection Readiness, Clinical Systems, CTMS, TMF, ePRO, IVRS, Central Labs, Imaging, Translation, Ancillary Supplies