The Clinical Research Physician will provide medical coverage for the Labcorp Drug Development 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
Minimum of 3-5 years medical practice experience
Experience with clinical drug trials highly preferred