The candidate will be responsible for project management support and facilitating the start-up activities of therapeutic oncology-based investigator-initiated trials (IITs) to ensure timely activation. Responsibilities include having a strong knowledge of clinical trial regulatory and compliance processes, communicating expectations as they relate to IIT protocol development with numerous relevant stakeholders, and generating reports for IIT activation metrics. Serving as a member in the Research Compliance Office (RCO) department, the candidate may also be responsible for providing quality assurance oversight of clinical trials via monitoring and auditing trial progress in the event of an FDA inspection. Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position responsibilities. This is a hybrid position requiring in-person and remote work.Huntsman Cancer Institute is committed to cancer prevention, care, and survivorship for all communities within the area we serve which includes Idaho, Montana, Nevada, Utah, and Wyoming with impact worldwide. Partnerships with individuals, communities, and many other entities are crucial to our work. Huntsman Cancer Institute values cancer-related health equity, and inclusion as integral to our guiding principle to serve our patients and their communities, and our commitment to foster a culture of belonging for all within our organization.In your cover letter or during your interview process, we invite you to share how your personal and professional experiences have prepared you to serve as a member of our team as we work to reduce the cancer burden experienced by all people and communities. This may include description of your prior experiences related to research, prevention, clinical care, community engagement/outreach, training, administration, or other areas relevant to Huntsman Cancer Institutes mission and this position.Learn more here