Heme/BMT Supervisor

Posting Description: Examples of Work Performed 1. Arranges orientation and provides training, supervision and leadership to the clinical research staff. 2. Assists clinical research staff with technical issues, problem solving and intervention when appropriate; delegates responsibility for elements of the conduct of selected clinical trials. 3. Acts as an interdepartmental liaison with UCH clinic staff (i.e. investigators, nurses, clinic support staff, laboratory, pharmacy, radiology). 4. Plans and directs investigator and coordinator meetings including but not limited to pre-study qualification visits, initial orientations, study audits, and closeout visits. 5. Responsible for all clinical research personnel issues, including performance evaluations, counseling, and disciplinary actions with guidance from Clinical Research Manager. 6. Works with finance team members to resolve discrepancies and to review account balances on a regular basis. 7. Participates in external audits and internal process improvement strategies to promote consistent best practices.

Minimum Qualifications: Education: BS or BA in Biology, Chemistry, Behavioral Science, Nursing or other related discipline. Experience: *Proficient with CRC III duties/responsibilities: Has served as primary coordinator for clinical trials, has experience in teaching, precepting and mentoring new employees to clinical research, has assisted in the development of policy, procedure or patient education materials related to clinical research *Three years of clinical and/or clinical research experience -OR- Any equivalent combination of Education or Experience Certification & Licensure Required: Clinical Research Certification (CCRC, CCRA, CCRP, RAC) or eligible to sit for next offered exam (2 years consecutive clinical research experience). Current Colorado State R.N. License (if applicable), CPR, CITI and HIPPA certification

Required Competencies/Knowledge, Skills, and Abilities: 1. Knowledge of basic human anatomy, physiology, medical terminology. 2. Advanced knowledge of Good Clinical Practices, FDA Rules and Regulations in relation to clinical trials, NIH guidelines, ICH guidelines and HIPAA regulations in relation to clinical trials, and NCI common toxicity definitions. 3. Understands the phases and concepts of clinical trials and the overall philosophies of conducting cooperative group research as they differ with NCI sponsored, private industry and investigator initiated clinical trials.

Desired Qualifications: *One year of oncology research *One year of personnel management experience

Campus: Anschutz Medical Campus