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Orange, CA
PROTOCOL DEVELOPMENT SPECIALIST - 10024796
Irwindale, 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 the Beckman Research Institute of 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.
Join City of Hope as a Protocol Development Specialist (PDS) and play a vital role in cutting-edge research. Collaborate with clinical researchers under OCPD Senior Manager's guidance to develop, write, and edit diverse clinical research protocols. Shape the future of medical research in a dynamic environment. The position is fully remote.
As a successful candidate, you will:
· Assist investigators in developing, writing, and editing clinical research protocol documents
· Collaborate with stakeholders for document development through various channels
· Expand non-scientific sections of protocols with minimal supervision
· Communicate with sponsors or academic partners for protocol templates and study facilitation
· Review and edit protocol background sections, ensuring submission readiness
· Provide excellent customer service with timely responses in document production
· Develop or review informed consent documents
· Coordinate responses during the protocol approval process, interfacing with internal stakeholders
Your qualifications should include:
· Master's degree or Bachelor's degree with a minimum of 3 years of relevant experience
· 1 years of relevant experience required
· Use of clinical research protocols
· Composition of therapeutic research protocols
· Regulatory work related to clinical protocols and development of informed consents
City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here.