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University of California - San Francisco

Clinical Research Coordinator - Immunox / Immunology / Collaborative Research

University of California - San Francisco, San Francisco, California, United States, 94199


Clinical Research Coordinator - Immunox / Immunology / Collaborative Research

Department of PathologyFull Time79970BRJob SummaryThe Bakar ImmunoX Initiative is an ambitious, first-in-class program at UCSF that uses social engineering, state-of-the-art technologies and infrastructure, and a unique data-sharing model to support a large community of researchers and clinicians as they seek to harness immunology to improve human health. By restructuring traditional research, we create opportunities for cross-fertilization of ideas, discoveries, and insights.UCSF's ImmunoX Office for Collaborative Research (OCR) is seeking a highly motivated and experienced Clinical Research Coordinator (CRC) to join our cross-functional team in a full-time capacity. The ideal candidate will play a critical role in clinical-translational research projects, acting as a link between the clinicians, research teams, study participants, and regulatory authorities. The chosen candidate's responsibilities will encompass various aspects of the research process, from study initiation to completion.The CRC's scope of duties encompasses, but will not be limited to, supporting the management and coordination of various clinical-translational research projects, with the level of involvement varying based on the projects' scale and intricacy. These projects may include, but are not limited to, biospecimen acquisition, chart review, interventional studies, and other research modalities. The candidate must demonstrate adaptability and proficiency in managing a diverse array of study types and methodologies.Responsibilities for this position include:Acting as an intermediary between services and departments while overseeing data and specimen management.Managing and reporting on study results; creating, cleaning, updating, and managing databases and comprehensive datasets and reports.Managing OCR and Investigator'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.Participating in the review and writing of protocols to ensure institutional review board approval within University compliance.Helping assure compliance with all relevant regulatory agencies; overseeing study data integrity; implementing and maintaining periodic quality control procedures.Interfacing with departments to obtain UCSF approval prior to study initiation; maintaining all regulatory documents; reporting study progress to investigators.Participating in any internal and external audits or reviews of study protocols; performing other duties as assigned.Note:

This position requires a physical/health screening.Required QualificationsHS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.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.Preferred QualificationsBA or BS in physical or biological sciences and one year of clinical research experience preferred.Fluency in the usage 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 and a relationship, while also giving insight to what is realistic and appropriate for patient participation.Experience with electronic medical records.Experience with REDCap database design and data entry.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.About UCSFThe 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. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences.Pride ValuesUCSF 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 - also known as our PRIDE values.Equal Employment OpportunityThe 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.OrganizationCampusJob Code and Payroll Title009335 CLIN RSCH CRDJob CategoryResearch and ScientificBargaining UnitUniversity Professional Technical Employees - Research Support Professionals Unit (UPTE-RX)Employee ClassCareerPercentage100%LocationParnassus Heights (SF)ShiftDaysShift Length4 HoursAdditional Shift DetailsMonday - Friday, 8:00am - 5:00pm

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