Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Clinical Research Coordinator

$83.49k - $95.91k
Full-time

UCSF

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.

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.

Responsibilities

%

of time ( Nothing less than 5%)

Essential Function (Yes/No )

Key Responsibilities

(To be completed by Supervisor)

20%

YES

Study Coordination and Data Collection

  • Identify subjects, develop recruitment and retention strategies, and screen and enroll study subjects.
  • Schedule subjects for study visits; meet with them to administer questionnaires, collect medical history and perform study procedures.
  • Maintain rapport and relationships with subjects to ensure effective communication and retention; respond to their diverse needs, schedule follow-up appointments, and become their intermediary; discuss study outcomes with providers to ensure continuity of care.
  • Obtain informed consent; review information with subjects; assess and advocate for patient safety throughout each protocol procedure.
  • Oversee subject reimbursement; work to resolve discrepancies and issues.
  • Work with staff to ensure procedures are completed, specimens properly stored, and required data collected at visits; and ensure correct shipping and labeling measures.
  • Coordinate, communicate and network with other studies and technicians to ensure scheduling efficiency;communicate with any affiliated groups.
  • Conduct reviews of medical charts and electronic records to extract medical information and other data for use in studies.
  • Implement needs assessments and recommendations for enhancements on patient coordination, data collection, data management, protocol adherence and study collaboration.
  • Assist with IRB protocols

10%

YES

Data management and reporting of results

  • Collect data during subject visits; enter data from visits, procedures, lab tests, and other subject-related participation into databases in a timely manner.
  • Manage database structure for each protocol; update databases to improve data analysis and management; create new databases as needed.
  • Create and maintain comprehensive data sets as requested by the CRC Supervisor and/or PI.
  • Maintain data collection forms for effective data collection, entry, and analysis.
  • Perform queries and analysis in databases.
  • Work with Supervisor to maintain complete and accurate data in the study database; analyze the data as they become available.

20%

Staff training

  • Help train staff and others on new research protocols, changes in procedures, study protocols, data collection/entry, database procedures, medical chart review and storage, and other procedures.
  • Attend and actively participate in regular team meetings

20%

YES

Quality control procedures

  • Oversee data integrity; initiate assessments of the adequacy of existing policies and procedures on subject recruitment, data collection, and data management.
  • Update and maintain a procedure manual documenting all study-related procedures; help develop a plan to ensure consistency in data collection and data entry.
  • Implement and maintain periodic quality control procedures

10%

YES

Study Implementation

  • Suggest modifications to the administrative infrastructure to accommodate increasing complexity of studies.
  • Modify data collection instruments
  • Help schedule staff time and coordinate staff schedules.
  • Maintain subject tracking systems.

10%

YES

Protocol Submissions and Adherence

  • Enter all existing and new study protocols into the Committee on Human Research (CHR) online system; seek assistance on maintaining all protocols in the system by communicating with CHR Analysts.
  • Design and enhance case report forms and data collection forms as needed; provide manuscript feedback; continue to develop and maintain systems for assuring protocol adherence and data quality.
  • Participate in the review and writing of protocols and related procedures to ensure institutional review board approval within University compliance.
  • Renew, modify, and submit CHR applications and protocols; ensure that protocol applications are submitted in a timely manner; serve as a liaison between CHR and study Investigators.
  • Provide quality assurance checks to note if protocols or UCSF CHR applications need to be modified; evaluate protocols on an ongoing basis and implement improvements as needed.

10%

YES

Regulatory responsibilities

  • Assure studies are carried out according to Code of Federal Regulations, Good Clinical Practice, and UCSF regulations.
  • Initiate and follow-up on CHR submissions and modifications; track approval status.
  • Interface with departments to obtain UCSF approval prior to study initiation.
  • Maintain regulatory documents; monitor timelines for data submission; document adverse events and submit to appropriate departments.
  • Use sound judgment to maintain patient confidentiality when communicating with agencies, healthcare providers, other studies, and outside departments.

Participate in and cooperate with any internal and external audits or reviews of study protocols; prepare necessary documentation.

100%

(To update total %, enter the amount of time in whole numbers (without the % symbol - e.g., 15, 20) then highlight the total sum (e.g., 1%) at the bottom of the column and press F9. The total sum should add up to 100%.)

Qualifications

Required Qualifications

  • HS 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.
  • Previous CRC experience

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.
  • 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 Professional
  • 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: 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 here.

Join us to find a rewarding career contributing to improving healthcare worldwide.

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:

Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Clinical Research Coordinator in Oakland, CA vacancy
  • $38.55 - $57.83 per hour

     ...System Office-ValleyPosition Overview: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... 
    Suggested
    Full time
    Work at office
    Shift work

    Sutter Health

    Oakland, CA
    4 days ago
  •  ...Mission Bay/Oakland Benioff Children's Hospital** 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... 
    Suggested
    Work at office
    Local area

    University of California - San Francisco

    Oakland, CA
    2 days ago
  • $145k - $165k

    Caribou Biosciences is a leading clinical-stage CRISPR genome-editing biopharmaceutical company dedicated to developing transformative...  ...documentation, timelines, trackers, and communications, while coordinating cross-functional development and review of key study... 
    Suggested
    Local area
    Remote work

    Caribou Biosciences

    Berkeley, CA
    7 hours ago
  • $185k - $195k

     ...Novartis and Mark Fishman, former President of the Novartis Institutes for Biomedical Research, the firm in-licenses promising therapies that for some reason are not advancing toward the clinic. The firm focuses on the translational phase of medicine to generate data that... 
    Suggested
    Full time
    Local area

    Aditum Bio

    Oakland, CA
    2 days ago
  • $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... 
    Suggested
    Contract work

    Amerit Consulting

    San Francisco, CA
    7 hours ago
  •  ...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... 

    Nudge Inc.

    San Francisco, CA
    2 days ago
  •  ...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 placement
    Local area

    UCSF Health

    San Francisco, CA
    4 days ago
  •  ...Clinical Research CoordinatorResponsibilities: Ensure each study patient is fully informed of the study at the time of the consent. Patient...  ....Must Haves: 1 - 10 experience as a Clinical Research Coordinator (sponsor-backed trials). Highly Preferred BA/BS in a scientific... 

    Connecting Talent 2 Opportunity

    San Francisco, CA
    3 days ago
  •  ...University of California - San Francisco is seeking a Research Compliance Analyst 2 to support oversight of human subjects, animal use...  ..., state, and University policies. Responsibilities include coordinating site monitoring visits, preparing for DSMC/IRB activities, assisting... 
    Worldwide

    University of California , San Francisco

    San Francisco, CA
    1 day ago
  • $38.55 - $57.83 per hour

     ...Office-Valley Position Overview: 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... 
    Full time
    Work at office
    Monday to Friday
    Shift work
    Weekend work

    Sutter Health

    San Francisco, CA
    5 days ago
  • 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... 
    Full time
    Shift work

    University-of-California---SAN-Francisc

    San Francisco, CA
    3 days ago
  • $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... 
    Hourly pay
    Full time
    Traineeship
    Work experience placement
    Casual work
    Work at office
    Immediate start
    Worldwide
    Monday to Friday
    Shift work

    University of California, San Francisco

    San Francisco, CA
    6 days ago
  • $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... 
    Hourly pay
    Full time
    Work experience placement
    Worldwide
    Monday to Friday
    Shift work
    Day shift

    University of California, San Francisco

    San Francisco, CA
    2 days ago
  •  ...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... 
    Work at office
    Worldwide
    3 days per week

    ICON Strategic Solutions

    San Francisco, CA
    4 days ago
  • $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 pay
    Work experience placement
    Worldwide
    Shift work

    University of California, San Francisco

    San Francisco, CA
    6 days ago
  • $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 pay
    Full time
    Work experience placement
    Worldwide
    Shift work

    University of California - San Francisco

    San Francisco, CA
    6 days ago
  •  ...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; Dr. Martinez); may coordinate... 
    Full time
    Work experience placement
    Worldwide

    University of California San Francisco

    San Francisco, CA
    4 days ago
  • $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 pay
    Full time
    Part time
    Work experience placement
    Local area
    Worldwide
    Shift work

    University of California , San Francisco

    San Francisco, CA
    3 days ago
  •  ...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... 
    Work experience placement
    Worldwide

    University of California , San Francisco

    San Francisco, CA
    2 days ago
  •  ...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 office
    Local area

    University of California , San Francisco

    San Francisco, CA
    3 days ago
  • 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 work
    Local area

    UCSF Health

    San Francisco, CA
    2 days ago
  • Caribou Biosciences, Inc. seeks a Clinical Trial Manager to drive operational execution for global trials in a fast-paced environment. You will oversee study start-up, site qualification, monitoring, data quality, and trials close-out, ensuring compliance with ICH-GCP... 
    Remote job

    Caribou Biosciences, Inc.

    Berkeley, CA
    6 days ago
  • $135k - $180k

    RONDO THERAPEUTICS CLINICAL TRIAL MANAGER (CTM)/Sr. CTM Rondo Therapeutics is a privately...  ...growth of our Hayward, California‑based research site. POSITION SUMMARY The Clinical...  ...forecasting and timing of resupply(ies). Coordinate biosample logistics with central and... 
    Full time
    Flexible hours

    Rondo Therapeutics

    Emeryville, CA
    2 days ago
  • $72 - $82 per hour

     ...aerosol delivery GENERAL SUMMARY: The Clinical Trial Manager will support the Company's...  ...periodic reviews Participate and coordinate resolution of audit finding and ensures...  ...: ~6+ years of clinical research experience within the Biotech or similar... 
    Hourly pay
    Full time
    Contract work
    Work experience placement
    Work at office
    Local area

    4D Molecular Therapeutics

    Emeryville, CA
    2 days ago
  • $120k - $135k

    DescriptionSummaryThe Clinical Trial Manager (CTM) will provide clinical study support to the Clinical Program Manager/Study Management...  ...cleaning activities with cross-functional teamMay lead and coordinate protocol deviation review and documentationManages clinical monitoring... 
    Contract work
    Work at office
    Remote work

    Arcus Biosciences

    Hayward, CA
    4 days ago
  • $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... 

    Galapagos NV

    San Francisco, CA
    7 hours ago
  • $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 pay
    Full time
    Work experience placement
    Worldwide
    Monday to Friday
    Shift work

    University of California, San Francisco

    San Francisco, CA
    3 days ago
  • $72.2k - $100k

     ...Job Description Job Description The Lead Site Clinical Research Coordinator (CRC) is the founding coordinator for Salma Health's Fremont clinic, responsible for establishing research operations at the site and managing day-to-day study conduct, including the ATLAS... 

    Salma Health

    San Francisco, CA
    20 days ago
  • $25 per hour

     ...Job Description Job Description Irvine Clinical Research is the largest independent memory research center on the West Coast. Alzheimer...  ...person to join our team as a Clinical Research Recruitment Coordinator. You will be speaking with potential study participants... 
    Hourly pay
    Full time
    Local area
    Remote work

    Irvine Clinical Research

    Oakland, CA
    a month ago
  • $120k

     ...(r2d2tbnetwork.org) is an international research consortium focused on accelerating the development...  ...in high TB-burden countries. The Clinical Trial Manager for the R2D2 TB Network...  ...and processes to lead, manage, and coordinate the conduct and reporting of multicentric... 
    Full time
    Work experience placement
    For subcontractor
    Worldwide

    UCSF

    San Francisco, CA
    5 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Clinical Research Coordinator. Be the first to apply!