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STUDY ADMINISTRATOR - 10029908
Duarte, CACity of Hope is an independent biomedical research and treatment center for cancer, diabetes and other life-threatening diseases.
Founded in 1913, City of Hope is a leader in bone marrow transplantation and immunotherapy such as CAR T cell therapy. City of Hope’s translational research and personalized treatment protocols advance care throughout the world. Human synthetic insulin, monoclonal antibodies and numerous breakthrough cancer drugs are based on technology developed at the institution. AccessHope™, a wholly owned subsidiary, was launched in 2019 and is dedicated to serving employers and their health care partners by providing access to City of Hope’s exceptional cancer expertise.
A National Cancer Institute-designated comprehensive cancer center and a founding member of the National Comprehensive Cancer Network, City of Hope is ranked among the nation’s “Best Hospitals” in cancer by U.S. News & World Report and received Magnet Recognition from the American Nurses Credentialing Center. Its main campus is located near Los Angeles, with additional locations throughout Southern California and in Arizona.
Join the forefront of groundbreaking research at City of Hope where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.
A Study Administrator position is currently available in the department of Population Sciences.
As a successful candidate, you will:
- Manage a team of research staff for multi-center research study and/or multiple research studies.
- Compilate, register and submit study data. Monitor project databases and maintain a system of effective data flow associated with research protocol(s).
- Facilitate and manage multi-faceted data collection projects, which include preparation and quality control of the data as well as result tabulation.
- Takes a lead role in preparing for IRB review of protocol(s) or maintaining continuing IRB approval of protocol(s), as well as assisting study staff to maintain regulatory compliance.
- Oversee DPS Clinical Research Assistants (CRAs) and/or Phlebotomists’ specimen and data collection activities.
- Maintain a system for effective study management and tracking of data and specimen collection.
- Serve as a resource for CRAs and/or Phlebotomists, and as a liaison between faculty, staff and other sites.
- Serve as a technical resource for the assigned project and assists in training new staff members.
- Be able to function independently and proficiently as defined in the position accountabilities.
Your qualifications should include:
- Bachelor’s Degree or Certified CRA or Certified Tumor Registrar in lieu of degree.
- Experience may substitute for minimum education requirements.
- At least three years’ experience working in clinical research, medical research, or public health, or related field.
- Experience managing multiple tasks.
Preferred education, experience and skills:
- Master’s Degree.
City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.
City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here.
To learn more about our Comprehensive Benefits, please CLICK HERE.