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
$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...SuggestedContract work$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$43.34 - $65 per hour
...Job Opportunity At Sutter Health Collects, compiles and presents clinical data for assigned area, ensuring accuracy, timeliness and accessibility of information. Maintains clinical and/or research databases for identified programs/ specialty clinics. Collects data used...SuggestedFull timeWork at officeMonday to FridayShift workWeekend 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 placementWork at officeWorldwide
$38.23 - $42.21 per hour
Job Summary 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...SuggestedHourly payFull timeTraineeshipWork experience placementCasual workWork at officeImmediate startWorldwideMonday to FridayShift work$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$34.32 - $55.19 per hour
...Neurology is seeking a bright, hardworking individual with strong communication and organizational skills to serve as a Clinical Research Coordinator. Within the Multiple Sclerosis (MS) group and under the supervision of the Clinical Research Manager or Principal Investigator...Hourly payWork experience placementWorldwideShift work- ...integrated effort building cutting-edge hardware, software, and research capabilities to create products that can benefit millions — and... ...Serve as the main point of contact for participants in clinical trials Assist with adverse event documentation and reporting...
$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- ...Job Description 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...Contract workLocal area
- ...ZSFG) is an internationally recognized global leader in HIV clinical care, research and education. It encompasses a network of specialty... ...clinical and translational research. The Clinical Research Coordinator (CRC) will work at an independent level to assist Principal...Work experience placementWork at officeAfternoon shiftEarly shift
- The Helen Diller Family Comprehensive Cancer Center (HDFCCC) is seeking a Clinical Research Coordinator to join the Pediatric Oncology/Hematology research team. The coordinator will independently execute, manage, and coordinate research protocols under the direction of...Work at office
- 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...
- Overview The Helen Diller Family Comprehensive Cancer Center (HDFCCC) seeks a Clinical Research Coordinator to join the Pediatric Oncology/Hematology research team. The Coordinator will independently execute, manage, and coordinate research protocols, under the direction...Work experience placementWork at officeLocal areaWorldwide
- Job Summary Senior Clinical Research Coordinators in the Cutaneous Oncology program independently coordinate and are accountable for the overall administration of one or more clinical studies. They provide advanced‑level knowledge, skills, and leadership to support clinical...Contract workLocal area
- ...Principal Investigator (PI) and Co-Investigator (Co-I), the incumbent will perform entry-level duties related to support and coordination of clinical research studies evaluating school-based behavioral interventions for children with ADHD. This position provides an opportunity...Work experience placementLocal areaWorldwideFlexible hoursAfternoon shiftEarly shift
$30.8 - $33.32 per hour
Job Summary 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...Hourly payFull timeWork experience placementWorldwideMonday to FridayShift work$60k - $140k
...Job Summary Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team! This is an exciting home-based opportunity for clinical research professionals with at least one year of Clinical Research Coordinator experience to fill Clinical Research...Full timeContract workTemporary workWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hours- ...further discussion.Job DescriptionThe Senior Clinical Trial Manager will independently manage... ...to and supports the company’s research and development efforts to create high value... ...provided upon database lock. Project and coordinate study supply and packaging requirements....Work at officeImmediate start
$150k - $170k
This is a rare chance to step in as the in‑region clinical operations lead for APAC at a privately backed, clinical‑stage biotech entering a decisive phase of growth. The company has moved beyond platform promise into execution - multiple programs advancing, real patients...Interim role$146.54k - $189.64k
...in cancer therapies, and help shape where our business and medical science goes next. Job Responsibilities Coordinating and supervising all aspects of a clinical study, including monitoring clinical trial sites. Assisting the Clinical Program Manager in overall study management...Contract workInterim roleLocal area- Under the supervision of the Clinical Research Manager, Clinical Research Coordinators (CRC) support the clinical trial management of investigator-sponsored, pharmaceutical-sponsored, and/or other types of consortium trials programs as assigned/needed. Responsibilities...Remote work
$140k - $170k
Braveheart Bio is a clinical-stage biopharmaceutical company focused on developing therapies for patients with hypertrophic cardiomyopathy... ...aiding in site selection, study implementation, and ongoing coordination of study sites, either directly or via CROs. Assist Clinical...Interim roleRemote workFlexible hours$120k - $150k
Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers... ..., Clinical Operations, you will be responsible for Contract Research Organization (CRO) oversight and execution of Revolution Medicines...Full timeContract workFor contractorsInterim roleLocal area- .... The HDFCCC integrates the work of researchers and clinicians dedicated to four fundamental... ...into the causes of cancer progression; clinical research to translate new knowledge... ...Job Summary: The Clinical Research Coordinator will perform independently or with general...Full timeWork experience placementWork at officeLocal areaWorldwide
- ...The Department of Otolaryngology-Head and Neck Surgery is recruiting a Clinical Research Coordinator (CRC) for the Children's Communication Center (CCC). The CRC will provide operational and research expertise to support the clinical, translational, outreach, publicity...Full timeFor contractorsLocal area
- ...The Clinical Research Coordinator (CRC) will join the Morrison Lab within the UCSF Department of Radiology and Biomedical Imaging. Neuroimaging research conducted within the Morrison Lab is focused on the application of magnetic resonance imaging (MRI) techniques to neuromodulation...Full timeWork experience placementWorldwide
- ...The Airway Clinical Research Center (ACRC) integrates research programs in asthma, COPD, sarcoidosis, and cystic fibrosis, along with current... ...and the pharmaceutical industry. The Clinical Research Coordinator will perform independently or with general direction at the...Full timeWork experience placementWork at officeWorldwide
- ...The Autopsy Coordinator will assist with the Memory & Aging Center Autopsy Program and the... ...maintaining contact with the cohort of living research participants and disseminating pathology... ...(MAC) is an internationally renowned clinical research center with a diverse workforce...Full timeTraineeshipWork experience placementImmediate startRemote workWorldwideWeekend workWeekday work
- ...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
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