The Clinical Research Physician will provide medical coverage for the Covance Clinical Research Unit (CCRU). As Principal Investigator/SubInvestigator, he/she is responsible for assuring the health and welfare of participants, performing medical procedures, ensuring proper conduct of the study trial, responding to all related medical decisions.

Duties and Responsibilities:

• Responsible for protecting the rights, safety and welfare of participants under their care.
• Responsible for ensuring that the clinical trial is conducted according to the investigational plan and all applicable regulations.
• Provide medical and scientific feasibility of all new sponsor inquires.
• Direct test article administration or dispensation.
• Review and evaluate protocols and provide clinical and scientific support.
• Liaise with sponsor regarding study design and site capabilities.
• Interact with regulatory bodies as is relevant to clinical operations.
• Attend study initiation meetings.
• Present protocols at IRB/IEC meetings, as required.
• Assist Operations and Client Managers with sponsor visits.
• Perform pre-study physical examinations and review lab data to ensure volunteers are medically and mentally fit upon entering the study.
• Perform on-study and post-study physical examinations to ensure that the physical and mental well being of volunteers is undiminished at the end of the study.
• Inform Principal Investigator, IRB and Sponsor as appropriate of relevant events.
• Review and sign CRFs at the conclusion of the study.
• Delegate the above as appropriate.
• Act as Principal Investigator/Co-Investigator as assigned by the Medical Director
• Weekend and off-hours work as necessary

• Active and unrestricted Wisconsin Medical License
• DEA license ideal
• CPR/AED Certified

• Minimum of 3-5 years medical practice experience
• Experience with clinical drug trials highly preferred