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Hybrid Clinical Project Director I
Location: US-NJ-East Hanover
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TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our pharmaceutical and healthcare clients, whose purpose is to reimagine medicine to improve and extend people's lives. They use innovative science and technology to address some of society's most challenging healthcare issues. They discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. Job Title: Clinical Project Director I Work Location: East Hanover, NJ 07936 -
As the leader of the cross-functional Clinical Trial Team (CTT), leads planning and management of the assigned clinical trial(s) end-to-end to achieve Global Program Team(GPT), Global Clinical Team (GCT), CTT and GDO-TM objectives. Oversees the conduct of clinical trial(s) including budget and resource allocation within assigned trial(s). Drives operational excellence through process improvement and knowledge sharing across trials. Enables an empowered organization that can navigate in a matrix environment and adjust quickly to business needs. Point of escalation for resolution of trial management operational issues within assigned trial(s). -
Builds best talent and an inspired, curious and empowered culture to foster high performance in a matrix environment. -
Responsible for overall management of trial management associates working on assigned clinical trial(s) including hiring, training, coaching, capability building, performance management and career development.
Assigns study responsibilities to assist in the planning, conduct and reporting of clinical trials.
Drives functional excellence in education, implementation and compliance to best practices and shares lessons learned for trial management. -
Contributes to cross functional activities and functional initiatives, when appropriate. Leader of the Clinical Trial Team -
Leads and manages the global cross-functional CTT to ensure deliverables are met within the established timelines, budget and quality/compliance standards; accountable for representation at all internal meetings related to the clinical trial; chairs the CTT meetings, participates and reports study progress and issues/resolution plan at the GCT, as extended member of the GCT. -
Drives CTT to plan and adapt innovative solutions that future-proof our clinical trials. -
Drives the implementation, maintenance and resolution of clinical trial quality risk management process within the CTT. -
Ensures escalation of appropriate trial risks and issues to the program level. -
Provides oversight on quality and compliance for assigned clinical trial(s) in conjunction with relevant line functions. Trial planning, execution and close-out: |
