BA/BS with a major in health science, RN or related field and six years of experience in administrative analysis or operations research; or an equivalent combination of education and experience; 5 years of experience in clinical research, clinical coordinator, clinical nurse role or an equivalent combination of education and experience; in-depth knowledge of FDA/ICH guidelines and significant experience managing clinical trials in academic clinical research or pharmaceutical/biotechnology company; expert knowledge of MS Office Suite; working knowledge of MS Project; knowledge and experience with medical and scientific terminology and concepts; effective communication and interpersonal skills; demonstrated ability to prioritize and multitask to meet multiple deadlines; ability to work independently and as part of a team; fluency in English (oral and written).
Preferred Qualifications:
Clinical Trials Professional certification; Clinical Trials project management experience; knowledge of UC/UCSF and NIH policies and procedures; experience in Diabetes, Allergy, Autoimmune Disorders, or Transplant.