Clinical Project Manager

Description:

The clinical project manager directs Phase I - IV clinical trials. Responsibilities include:

	designing, communicating and implementing project plans
	facilitating budget and contract development
	tracking projects and managing timelines
	overseeing contracted activities
	managing matrix teams and processes to ensure the progress of clinical trial development and implementation

Requirements:

	B.S. and/or M.S. in healthcare-related field
	CRO or pharmaceutical company project management experience
	proven team management experience
	proven administrative management of long-term study
	proactive problem-solving skills
	ability to multi-task, meet rigorous timelines and deal with stressful situations
	significant development process knowledge and experience, including study initiation procedures, clinical monitoring functions, drug safety and regulatory affairs issues, data flow, analysis and report generation, and FDA regulatory requirements (GCPs, CRFs, etc.)

Position involves travel about 20% of work time.

To apply for one of the above positions, please submit your résumé or curriculum
vitae (CV) to careers@researchpoint.com