MED-ZSFG-PULM

Full Time

75574BR

Job Summary

The Clinical Research Coordinator (CRC) will support with the following research studies:
"Collaborative Approaches to Examining Adversity and Building Resilience" (CARE) program. The CARE study brings together a cross-discipline, cross-sector team to study how to enhance resilience in children and families who have weathered substantial adversity. This study aims to understand how stress "gets under the skin" and how resilience-promoting caregiver-child interventions may mitigate the negative health effects of adverse childhood experience. We are recruiting families to an intervention study designed to improve child-caregiver bonding and resilience, caregiver stress and child behavioral outcomes, and biologic measures of stress.
adolescents aged 8-16 years old with physician-diagnosed asthma. The study involves the collection of multiple types of data, including demographic, medical history, measures of psychosocial stress, handling and shipment of biospecimen (nasal and oral swab, blood), and physiological testing (anthropometry, blood pressure measurement, lung function testing).
The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Incumbent's duties may include, but will not be limited to supporting the management and coordinating 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, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage 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; participate in the review and writing of protocols to ensure institutional review board approval within 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 CRC's duties may include, but will not be limited to:

• recruiting research subjects by telephone or in-person,
• abstracting information from clinical records and conducting structured chart review,
• conducting screening and obtaining informed consent,
• conducting cross-sectional and longitudinal quantitative and qualitative interviews in person and by telephone,
• administering surveys,
• tracking and scheduling study participants for interviews or visits,
• analyzing collected data using quantitative and qualitative methods,
• conducting literature searches,
• abstracting information from clinical records, transcripts and journal articles,
• supporting the management and coordinating the tasks of multiple clinical research studies,
• managing and reporting on study results,
• creating, cleaning, updating, and managing databases and comprehensive datasets and reports,
• managing 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,
• preparing research reports,
• participating in any internal and external audits or reviews of study protocols,
• leadership of and participation in community events at affiliated institutions.

To see the salary range for this position (we recommend that you make a note of the job code and use that to look up):

Please note: The compensation ranges listed online for roles not covered by a bargaining unit agreement are very wide, however a job offer will typically fall in the range of 80% - 120% of the established mid-point. An offer will take into consideration the experience of the final candidate AND the current salary level of individuals working at UCSF in a similar role.

For roles covered by a bargaining unit agreement, there will be specific rules about where a new hire would be placed on the range.

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Department Description

The Pulmonary Division at Zuckerberg San Francisco General Hospital is committed to improving the care and health outcomes among disadvantaged populations locally and globally. The purpose of the Clinical Research Coordinator position is to carry out the needed tasks as part of ongoing and future clinical and translational research projects to address social adversities and bolster resilience in socially vulnerable communities in the San Francisco Bay Area.

Required Qualifications

• HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.
• Must be a fluent Spanish speaker in both written and verbal Spanish. Must be able to translate English into Spanish and vice versa, and be able to conduct in-depth, complex interviews in Spanish
• Creating a welcoming, inclusive, and supportive environment
• Experience working with culturally and linguistically diverse groups
• Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, and other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population.
• Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.
• Demonstrate excellent attendance and reliability. Willingness to work during some evening and weekend hours required.
• 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 Qualifications

• Demonstrated ability to develop recruitment strategies in complex environments and differing patient pools, independently identifying recruitment leads, implementing new strategies, and continually adjusting strategies to meet current recruitment goals.
• Two years' experience in conducting research in community health setting
• Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.
• Experience in clinical pulmonology and clinical/epidemiology/pulmonary research
• 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.
• Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA 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: REDCap, Access, Stata, SASS/ SPSS, and Teleform programming platforms.
• 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 Safety Training

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. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world's leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.

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 - also known as our PRIDE values.
In addition to our PRIDE values, UCSF is committed to equity - both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available at
Join us to find a rewarding career contributing to improving healthcare worldwide.

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.

Organization

Campus

Job Code and Payroll Title

009335 CLIN RSCH CRD

Job Category

Research and Scientific

Bargaining Unit

University Professional Technical Employees - Research Support Professionals Unit (UPTE-RX)

Employee Class

Career

Percentage

100%

Location

Various Work Sites

Shift

Days

Shift Length

8 Hours

Additional Shift Details

M-F 9am-5pm