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RESPONSIBILITIES

Responsibilities: designing, directing and monitoring human clinical trials, phases II-IV, for pharmaceutical products under development, mainly in the field of Hepatitis C. Lead protocol team activities inc. planning, execution, and interpretation of clinical trials and data collection activities. Other responsibilities inc. interactions with regulatory agencies, Key Thought leaders, and site investigators. Serve as a medical expert to marketing or research teams, and oversight of writing of scientific publications.

REQUIREMENTS

Board Certified MD or MD, PhD; prefer expertise in hepatology, infectious diseases, or immunology; prefer 3-5years clinical/R&D industry experience
Developing a network of individuals from various departments important to job function - Interact with key academic investigators in hepatitis, virology or immunology, as well as site investigators
Training, knowledge and some experience in of early drug development preferred
Experience in clinical medicine and monitoring for safety in a clinical setting
Strong interpersonal skills required
Excellent written and verbal communication skills

LOCALE

New Haven, CT

HOW TO APPLY

To apply for this position, copy/paste the following URL into your browser: http://ars2.equest.com/?response_id=5db8fbbcbffb82cf0c9e6495cd12eb9b

DEADLINE

March 7, 2011

Discussion forums: Opportunity: Director / Study Director (#1100282) @ Bristol-Myers Squibb--New Haven, CT (US)

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