Clinical Research Coordinator
2 days ago
Division of Cardiology
Full Time
82092BR
Job Summary
The Cardiovascular Genetics Center within the Department of Medicine, Division of Cardiology has developed a clinical research infrastructure. The goals are to leverage our considerable case volume of patients referred for genetic testing and inherited cardiovascular disease to create a system that will allow for investigator-initiated research studies, to develop a cardiovascular genetics cohort studies, to facilitate contributions to multicenter registries, and to facilitate translational and/or industry-sponsored research on novel therapies. 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, clinical genetic counselors, the Director of Clinical and Translational Cardiovascular Genetics Research, and/or the Principal Investigator (PI), 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. This position will involve interacting with patients with inherited cardiovascular disease and their families, including obtaining informed consent for study participation.
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; assist with training of Assistant CRCs if needed, 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.
Department Description
The Division of Cardiology is one of the largest clinical, research and training divisions of the Department of Medicine (DOM) at UCSF. The Division has developed a well-established Cardiology Clinical Research Unit (CCRU) which supports 60-70 active clinical trials. The CCRU research portfolio covers phase I- IV and post approval trial types and covers a diversity of trials ranging from pharmaceutical, device, preventative, and social behavioral research.
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.
Preferred Qualifications
- Strong interest in genetics and cardiology.
- Undergraduate degree in a health sciences related discipline.
- Experience in clinical cardiology and clinical/cardiovascular research.
- Science, research, or medical background.
- Understanding of patient population to create rapport, while also giving insight to what is realistic and appropriate for patient participation.
- Experience with electronic medical records.
- 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.
- Knowledge of programming, data management, and database building within some of the following: R, Python, Excel, Access, Stata, SASS/ SPSS, and Teleform programming platforms.
About UCSF
The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care.
Pride Values
UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence.
Equal Employment Opportunity
The University of California San Francisco is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information.
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