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 at a large pharmaceutical company. Strong knowledge of ICH-GCP and local regulatory requirements is essential.

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, Project Management, Life Sciences, ICH-GCP, Regulatory Requirements, Trial Management, Vendor Management, Budget Oversight, Training Materials, Investigator Meetings, Health Authority Inspections, Data Management, Monitoring Guidelines, Central Trial Activities, CAPA Processes, Enrollment Commitments, Trial Documentation, Stakeholder Engagement, Inspection Readiness, Cross-Functional Teams, Trial Milestones, Recruitment Plans, Out-of-Pocket Costs, FTE Cost Drivers, Virtual Team Coordination, Analytical Skills, Communication Skills, Decision-Making Skills, Problem Solving, Therapeutic Area Expertise