Clinical Research Coordinator
UCSF Health
Job Description 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 Clinical Research Supervisor and/or 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. The 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 other team members, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; enter study data into databases and check data entry for quality assurance, participate in project team meetings, evaluate eligibility criteria for research participation for report to study PI, enroll/register/schedule/retain study participants, collect clinical data and shipment of biological samples, ensure participants are evaluated according to study protocol, 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. Department Description The UCSF Department of Psychiatry and Behavioral Sciences (DPBS) is among the nation's foremost resources in the field of child, adolescent, and adult mental health. Psychiatry faculty members are recognized for their leadership roles in state-of-the-art, comprehensive, and compassionate patient care, pioneering research, excellence in training the next generation of leaders, advancing public policy to advance mental health, and commitment to diversity. Department programs are active at all major UCSF campuses. Qualifications HS degree or equivalent 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. Excellent presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team. Proficiency with Microsoft Word, Excel, PowerPoint, and Windows. Excellent analytical and problem‑solving skills. Ability to work effectively in a fast‑paced, team‑based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects. Ability to establish cooperative working relationships with patients, co‑workers, & physicians. Experience with geriatric, medical, or public health patient populations. Basic knowledge of social science research design and statistical analyses. Research interviewing experience with structured psychiatric instruments and/or disability measures. Experience administering neuropsychological tests with older adults. Recruitment experience with older adults and psychiatric patient populations. Preferred Qualifications Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system. Bachelor’s Degree in Psychology or Neuroscience. Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation. Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals. 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 (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. 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 Demonstrated proficiency with medical terminology. Experience working with patients or study subjects. Prior experience with use of neuropsychological, psychological and disability measures in older adults Knowledge about and previous experience with mental health issues in older adults. Knowledge of local mental health facilities and resources. Knowledge of relevant literature regarding older adults, Hoarding Disorder, and Late Life Depression. Clinical education/experience. Experience with SPSS statistical package. Experience with EndNote program Knowledge of statistics Experience scheduling neuroimaging scans and neuroimaging protocols Equal Employment Opportunity The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law. Salary Information 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. To learn more about the benefits of working at UCSF, including total compensation, please visit #J-18808-Ljbffr UCSF Health
$34.32 - $55.19 per hour
...Job Summary The Clinical Research Coordinator will independently execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI). The role involves coordinating data collection and operations of multiple...SuggestedHourly payFull timeWork experience placementWorldwideMonday to FridayShift workDay shift- ...integrated effort building cutting-edge hardware, software, and research capabilities to create products that can benefit millions — and... ...metricsServe as the main point of contact for participants in clinical trialsAssist with adverse event documentation and reportingAssist...Suggested
- ...that benefit patients worldwide. What you will be doing: The Clinical Trial Assistant is a member of the clinical trial team supporting... ..., SAEs, protocol deviations and more as needed per study Coordination and tracking of clinical supplies Coordinate and arrange internal...SuggestedWork at officeWorldwide3 days per week
- ...The Clinical Research Coordinator (CRC) is responsible for independently managing and coordinating clinical research studies within the UCSF Fein Memory and Aging Center. Under the direction of the Principal Investigator (PI) and Clinical Research Supervisor, the CRC oversees...SuggestedFull timeShift work
- ...Job Description 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 Clinical Research Supervisor and/or Principal...SuggestedWork experience placementLocal area
$35 - $40 per hour
...more. Base pay range $35.00/hr - $40.00/hr Recruiting Manager/ Lead Engineering Recruiter at Amerit Consulting Position: Clinical Research Coordinator Duration: 5-6 Months + Strong Possibility of Extension Pay Rate: $35/hr - $40/hr (depending on experience) Job...Contract work- ...Clinical Research Coordinator Responsibilities: Ensure each study patient is fully informed of the study at the time of the consent. Patient recruitment responsibilities. Create source documents for study visits. Communicate closely with monitors, sponsors, and investigators...
- ...organized into brain networks across the lifespan. ALBA group research how language skills and brain regions are impacted by... ...will perform entry-level duties related to the support and coordination of clinical studies of participants with language difficulties enrolled...Full timeWork experience placementWorldwide
- ...JOB SUMMARY The Clinical Research Coordinator (CRC) will provide research coordination for the UCSF ID Clinical Research Center (SF IDRC), within the HIV, Infectious Diseases and Global Medicine (HIVIDGM) Division. Our unit conducts new and ongoing clinical trials...Full timeWork experience placementWork at officeLocal areaWork from homeWorldwideWeekend workAfternoon shiftEarly shift
- The UCSF Cutaneous Oncology clinical research team supports a diverse portfolio of studies for melanoma and non-melanoma skin cancers. The... ...Oncology to advance multidisciplinary care. The Clinical Research Coordinator will independently coordinate protocols under the direction...
- ...policies, projects, programs and issues in support of a function, research initiative, program and / or organizational unit, or in... ...Adolescent Depression Study, a randomized, placebo-controlled clinical trial examining the relationship between the gut microbiome, brain...
- Job Description 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 Clinical Research Supervisor and/or Principal...Work experience placementWork at officeWorldwide
- ...Under the supervision of the Clinical Research Supervisor, Clinical Research Coordinators (CRC) support the management of investigator-sponsored research studies as assigned/needed. Responsibilities include communicating with the Clinical Research Supervisor to ensure...Full timeWork experience placementWork at officeWorldwide
- ...The Airway Clinical Research Center (ACRC) integrates research programs in asthma, COPD, sarcoidosis, and cystic fibrosis, along with current... ...NIH) and the pharmaceutical industry. The Clinical Research Coordinator (CRC) will primarily be responsible for assisting with the...Work experience placementWork at officeWorldwide
- University of California, San Francisco is seeking an Assistant Clinical Research Coordinator to support the CHAMP program. The role focuses on coordinating research protocols, overseeing data and specimen management, and ensuring regulatory compliance under supervision...
$34.32 - $55.19 per hour
Clinical Research Coordinator Psych-Core-Rsch Full Time 83999BR Job Summary Dr. Christina Mangurian (PI) has received funding from the Department of State Hospitals (DSH) to direct a clinical research program related to the provision of mental health treatment/assessment...Hourly payFull timeWork experience placementWorldwideShift work- ...Department of Medicine, Division of Cardiology has developed a clinical research infrastructure within the Division. The goals are to... ...the incumbent will perform duties related to the support and coordination of clinical studies and may receive training and development...
- ...University of California - San Francisco is seeking a Clinical Research Coordinator to manage and coordinate research protocols under the supervision of the PI and Clinical Research Manager. You will oversee data collection, regulatory compliance, and overall study operations...
$41.72 - $67.1 per hour
...Senior Clinical Research Coordinator MED-VAMC-INFD Part Time 86545BR Job Summary Senior Clinical Research Coordinators independently coordinate and are accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge...Hourly payFull timePart timeWork experience placementLocal areaWorldwideShift work- ...Benioff Children's Hospital** Job Description The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator to join the Pediatric Oncology/Hematology research team. The Clinical Research Coordinator will perform independently to...Work at officeLocal area
- ...ZSFG) is an internationally recognized global leader in HIV clinical care, research and education and has grown to encompass a network of... ...clinical and translational research. The Clinical Research Coordinator (CRC) will work at an independent level to assist the...Full timeWork experience placementWork at officeLocal areaWork from homeWorldwideAfternoon shiftEarly shift
- ...with complex pulmonary disease and pulmonary infections. Research, including clinical trials of new therapeutics and prospective observational... ...mission. The program is seeking an Assistant Clinical Research Coordinator (aCRC) to assist with the daily operations of our...Work experience placementWorldwide
- ...purpose of the position is to help manage and execute all clinical and translational research studies for the Principal Investigators. Currently, the... ...has two multicenter studies, where UCSF is both the coordinating center and a clinical site, the other PIs have several...Full timeWork at officeLocal areaWork from home
- ...The Clinical Research Coordinator will work independently or under general direction by the Clinical Research Supervisor and/or Principal Investigator (PI) to manage and coordinate research protocols within the Department of Surgery Clinical Research Core. The coordinator...Full timeWork experience placementWorldwide
- ...Please note: This is a limited appointment with 18 months duration. Senior Clinical Research Coordinators independently coordinate and are accountable for the overall administration of one or more clinical studies, typically requiring advanced-level knowledge and skills...Contract workWork experience placementLocal areaWorldwide
- ...The Senior Clinical Research Coordinator independently coordinates and is accountable for the overall operation of the Ibrahim El-Hefni Liver Biorepository (IELB) and its associated clinical research studies at UCSF. Requiring advanced-level knowledge and skills, the...Full timeContract workWork experience placementLocal areaWorldwideFlexible hours
- ...submitting to the Institutional Review Board, and other study coordination duties. Please review the details about this role and... ...increasing the number of hours per week in the future The Clinical Research Coordinator (CRC) under general direction, independently manages...Part timeRemote workMonday to FridayAfternoon shift
- ...Job Summary: The Cutaneous Oncology clinical research team supports a diverse portfolio of studies for melanoma and non-melanoma skin... ...assessment, and long-term survivorship. The Clinical Research Coordinator (CRC) will independently, or with general direction, execute...Full timeWork at officeLocal area
$150k - $165k
...programs, led by a potential first‑in‑class clinical asset and complemented by an exciting... ..., study plans, and any other clinical research related documents, in collaboration... ...evaluate and approve vendor change orders, coordinating review and updates or revisions with...- ...Under the supervision of a Clinical Research Supervisor or Principal Investigator (PI), the incumbent will perform entry-level duties related to the support and coordination of clinical studies, and may receive training and development to prepare and advance for journey...Full time
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