(US-Massachusetts) Our client, a leader in clinical research, has an immediate need for an Associate Director of Clinical Monitoring, reporting to the President of the company. This highly visible position requires a candidate with strong leadership and team building skills. The Associate Director will be responsible for coordination and execution of clinical trial projects, interdepartmental collaborations, interaction with clients, developing and maintaining budgets for the department and sponsor contracts, manage timelines, scheduling and deliverables. REQUIREMENTS: *BS in life sciences; Master's preferred *5+ years experience in pharmaceutical, biotechnology or CRO industry *3+ years management experience; prefer 2+ years management experience in a CRO *Must have very strong management skills *Excellent knowledge of GCP, ICH guidelines and clinical monitoring processes and procedures. *Demonstrated ability to manage projects and staff Excellent communication and interaction skills at all levels of management *Able to travel up to 25%.
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