Physician / Medical Director / Ohio / Permanent / MEDICAL DIRECTOR/ASSOCIATE MEDICAL DIRECTOR needed in Medford, Oregon Job
Velocity Clinical Research
Cincinnati, OH, 45201, USA
Cincinnati, OH, 45201, USA
- Healthcare
- Full-time
- Medical Director
- Clinical Research
- Principal Investigator
This full-time Physician/Medical Director role is based at a clinical research facility in Cincinnati, Ohio, providing medical leadership and oversight for clinical trials. The position involves acting as Principal or Sub-Investigator, ensuring participant safety, regulatory compliance, and collaboration with pharmaceutical sponsors. Key duties include protocol review, patient recruitment support, clinical assessments, and contributing to the operational success of the research site.
This physician executive/ clinician full time opportunity is based at VCRs Cincinnati Ohio (New Horizons Clinical Research) clinical research facility. The position provides medical direction, strategy, and coverage for VCRs research services. Acting as a Principal Investigator or Sub-Investigator, the M.D. is responsible for assuring the health and welfare of study participants. In addition, the performance and oversight of medical procedures and the management of the proper conduct of studies/trials in accordance with regulatory guidelines and sound medical practice is a key responsibility. The incumbent works closely with pharmaceutical companies and other study sponsors to ensure complete medical continuity and study success throughout the research process.Key responsibilities include:Principal Investigator or Sub-Investigator as assigned Support the site Director in patient recruitment strategies to meet demanding enrollment targets and requirementsProtect the rights, safety, and welfare of study participantsProvide overall medical direction and medical review of protocols in conformance with the investigational plan and good clinical practiceProvide medical and scientific feasibility of all new sponsor inquiriesAttend study initiation meetings and present protocols at IRB meetingsAssist and provide guidance to clinical operations, research staff, and to sponsor client managers as required.Ensure that all clinical trials are conducted according to the investigational plan and appropriate regulationsClinical assessment and evaluation of study participantsAssist clinical site management and VCR executives in overall facility operation as required




