Program Operations Leader
This is a leadership role where you will oversee the operational strategy for delivery of one or more complex programs in Clinical Trial Management. You will be responsible for clinical operations activities and decisions, including quality, timelines, and budgets related to the conduct of clinical research studies.
You must have at least 12 years of experience in in-house sponsor-side pharmaceutical industry with 8 years in clinical operations. A Bachelor's degree is required.
Duties and Responsibilities:
* Maintain an overview of program status and issues, communicate progress risks issues changes that may impact quality timelines budget provide updates to stakeholders as requested
* Provide operational insight into feasibility timeline cost estimates during development Oversee study timelines within a program Provide input on protocol design feasibility start up phases Ensure consistency across teams Develop best practices
* Oversight vendor selection management drive decision making integrate all considerations ensure goals are attainable Act as point contact escalate review key metrics track study progress Create risk mitigation strategies Implement solutions cross functional teams Assist preparing scenarios creative solutions challenges Drive oversight CROs vendors deliverables relationships counterparts May require travel