drjobs Clinical Research Coordinator - Melanoma and Cutaneous Program

Clinical Research Coordinator - Melanoma and Cutaneous Program

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1 Vacancy
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Job Location drjobs

San Francisco, CA - USA

Hourly Salary drjobs

$ 34 - 55

Vacancy

1 Vacancy

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. Incumbents 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 Investigators 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 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.

This position is expected to start in May 2025.

The salary range for this position is $34.32 $55.19 (Hourly Rate).

To learn more about the benefits of working at UCSF including total compensation please visit: graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities.

  • Ability to work with a sensitive population of patients (oncology patients).
  • 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
  • multitask in a fastpaced 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
  • Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission renewal and modification of protocols through this system.
  • Demonstrated knowledge and understanding of research especially in the areas of biological sciences.
  • Exceptional database management experience and prior experience with various computer programs (Microsoft Office; internetbased databases) and using specialized software such as OnCore.
  • Experience with medical charts and electronic records.
  • Ability to sit and work at a computer for several hours per day. May need to travel between one or more campuses via UCSF shuttle. Ability to stand for several hours of the day.
  • Experience in clinical research or demonstrated research or training experience that translates into a clinical research setting.
  • Familiarity with specimen processing or demonstrated ability to learn specimen processing in a laboratory
  • environment.
  • Working knowledge of or demonstrated ability to learn federal state and local research regulations and
  • guidelines and research practice methods in a laboratory or clinical setting.
  • Ability to independently interpret and apply policies respond to requests resolve issues and provide
  • assistance to faculty and staff at all levels in a team oriented environment.
  • Ability to work across several different programs reporting to 23 different supervisors.


    • Bachelors degree with a major in science or related.
    • Understanding of patient population to create rapport and a relationship while also giving insight to what is realistic and appropriate for patient participation.
    • Prior analytical and writing skills in a science/research environment
    • Knowledge of clinical research in oncology preferably melanoma.
    • Knowledge and experience in managing oncology clinical trials and experience with Phase IIII trials.
    • Membership in a clinical research professional society.
    • Knowledge of location specific and departmental policies for dealing with reimbursement guidelines for research confidentiality and HIPPA regulations following the locations 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.


    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.

    Department Description
    The UCSF Helen Diller Family Comprehensive Cancer Center (HDFCCC) holds the prestigious designation of comprehensive from the National Cancer Institute (NCI). We combine basic science clinical research epidemiology cancer control and patient care throughout UCSF.

    About UCSF
    The University of California San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research graduatelevel education in the life sciences and health professions and excellence in patient care. It is the only campus in the 10campus UC system dedicated exclusively to the health sciences. We bring together the worlds 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.

    Required Experience:

    IC

    Employment Type

    Full Time

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