Clinical Research Coordinator Cardiology

Job Description The Department of Medicine, Division of Cardiology, has developed a clinical research infrastructure within the Division. The goals are to increase industry-sponsored research, create a system that supports physicians in operationalizing investigator-initiated studies, and develop a general cardiology cohort study. The purpose of this position is to carry out tasks as part of ongoing and future clinical and translational research projects within the Division of Cardiology. Under the supervision of the Clinical Research Supervisor or Manager, the incumbent will perform duties related to the support and coordination of clinical studies and may receive training and development to prepare for advancement to the next level within the series. Qualifications Required Qualifications HS graduate and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population. Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines. Demonstrated ability to exercise tact and discretion in sensitive communications with patients and others. Demonstrated ability in handling a variety of confidential information appropriately. Demonstrated positive interpersonal skills and problem solving abilities. Willing to travel (limited travel for investigator meetings) Preferred Qualifications Experience in clinical cardiology and clinical/cardiovascular research Science, research, or medical background Applied knowledge in drug and/or device trials A two-year commitment is preferred Proficiency in the use of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system. Understanding of patient population to create rapport, while also giving insight to what is realistic and appropriate for patient participation. In‑depth knowledge of ICH/GCP and FDA requirements for INDs, IDEs, and NDAs. Experience in building strong working relationships with Sponsors, Monitors, PIs, and other key stakeholders Experience with electronic medical records, EPIC preferred. Knowledge of biospecimen collection, processing, and transport Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPAA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms. Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals Experience applying the following regulations and guidelines: Good Clinical Practice Guidelines Health Information and Accountability Act (HIPAA) The Protection of Human Research Subjects CHR regulations for recruitment and consent of research subjects Effective Cash Handling Procedures Environmental Health and Safety Training #J-18808-Ljbffr