Senior Clinical Project Manager

Responsibilities Create, manage, and maintain integrated study schedule in MS Project, including Key Event Maps, Roadmaps, and critical path visualization aligning in Planisware. Assure Clinical timelines in Planisware align to MS Project schedule and coordinate the integrated clinical plan with Clinical Development Team project plans. Ensure proper resource demand is reflected. Develop scenarios in Planisware for budget, timeline and FTE forecasting, while generating situational operational scenarios. Collect, consolidate, and report financial, timeline and resource data for governance approvals and external funding partnerships. Manage scope control, FTE and Out of Pocket variances. Document key decisions, actions, risks, issues, and lessons learned, as well as maintain trial governance documentation. Ensure risks are captured and monitored. Ensure budgets are effectively managed and forecasts adjusted to reflect current thinking. Drive and facilitate after action review meetings and results are documented. Work with the team to assess and remediate impact to scope, budget, timelines. Provide support for team-based reporting. Mentor & support onboarding of new team members, particularly those in Trial Management. Requirements Education: Bachelor’s degree required Minimum of 4 years in Pharmaceutical, Healthcare or related industries Strong Project Management experience Must possess excellent leadership skills and proven ability to foster team productivity and cohesiveness Experience leading without authority and in multi-functional matrixed and global environments Excellent decision-making, analytical and strong financial management skills Strong communication and presentation skills Up to 10% travel – Domestic & International Preferred: Knowledge of Clinical Research Operations 2-3 years of experience managing multiple aspects of the execution of global clinical trials (Phases I-IV) #J-18808-Ljbffr