Job Details

Job SummaryThe 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 will assist a physician within the division to operationalize an investigator-initiated study, and to develop a general cardiology cohort study. The purpose of this position is to carry out the needed tasks as a part of ongoing and future clinical and translational research projects in the Division of Cardiology.Under the supervision of the Clinical Research Supervisor, the incumbent will perform duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance to the next level within the series.Incumbent's duties may include, but will not be limited to, support the management of and coordinate the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, update, and manage databases and comprehensive datasets and reports; help to coordinate staff work schedules to ensure proper coverage; assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage PI's protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval and University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned.The final salary and offer components are subject to additional approvals based on UC policy.Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.The salary range for this position is $37.12 - $59.69 (Hourly Rate).To learn more about the benefits of working at UCSF, including total compensation, please visit: 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* Fire/ Life Safety Training