Address
Form of workTriCore Research Institute seeks a Medical Director of Clinical Trials and Research.The Medical Director's primary role is to identify and deliver clinical device trials business opportunities that align with the strategic needs of the TriCore Research Institute (TRI) and serve as a Principal Investigator of clinical device trial studies. The Medical Director will focus on providing scientific, administrative, regulatory, and support on a wide range of clinical research studies. The Medical Director will work closely with the TRI Section Chief and other TRI leaders to analyze and prioritize new business opportunities, promote quality research, and ultimately increase the volume of Clinical Trials that will benefit TriCore and the customers it serves.The Medical Director will remain academically active through publishing in peer-reviewed journals, abstracts, and poster presentations and/or oral presentations at scientific and/or clinical meetings and conferencess that directly align with TriCore's strategic needs.
ESSENTIAL FUNCTIONS:1. Responsible for full scope of study conduct in collaboration with lab operations to ensureclinical and Research studies are conducted according to the Code of Federal Regulations,Good Clinical Practices, and local regulatory requirements.2. Contributes to protocol development and feasibility assessments including the writing ofstudy protocols, amendments, and administrative changes as applicable.3.
When serving as principal investigator, review and comment on sponsor contracts and protocols as applicable.4. Working within the appropriate management dyads and teams, Coordinate business opportunities for the start-up, implementation, and closeout of Clinical Trials.5. Planning and participation in investigator meetings in collaboration with team members.6.
Ensure clinical and Research studies meet sponsor timelines.7. Act as a resource for TRI leadership, investigators, and other staff through the provisionand promotion of appropriate training in the conduct of trials.8. Participate in strategic planning processes to establish and achieve long range TRI goals.9.
Represent TRI in internal and external meetings relating to strategic priorities.10.Develop and maintain mutually positive and beneficial relationships with study sponsors and clinical research organizations.11.Generate new business opportunities and proposals.12.Develops and implements effective strategies to analytically verify/validate clinical assays needed to support research studies.13.Publish scholarly works including manuscripts, abstracts, and/or scientific posters.The above statements describe the general nature and level of work being performed by individuals assigned to this classification. This is not intended to be an exhaustive list of all responsibilities and duties required of personnel so classified.Education: See Minimum QualificationsEmployment Type: Regular - Full Time
