What are the responsibilities and job description for the Associate Clinical Trials Management (Contract) position at Allogene Therapeutics?
Job Description
About Allogene :
Allogene Therapeutics, with headquarters in South San Francisco, is a clinical-stage biotechnology company pioneering the development of allogeneic chimeric antigen receptor T cell (AlloCAR T™) products for cancer and autoimmune disease. Led by a management team with significant experience in cell therapy, Allogene is developing a pipeline of “off-the-shelf” CAR T cell product candidates with the goal of delivering readily available cell therapy on-demand, more reliably, and at greater scale to more patients. For more information, please visit www.allogene.com, and follow @AllogeneTx on X (formerly Twitter) and LinkedIn.
About the role :
Allogene Therapeutics is seeking a highly motivated Associate Clinical Trial Manager to support the execution and oversight of Allogene’s Clinical Trials. This role will be responsible for providing administrative assistance to support key study conduct activities including but not limited to site selection, site management, study coordination, and regulatory compliance activities. This is a contract opportunity with possible intent to hire within the Clinical Operations team.
Responsibilities include, but are not limited to :
- Support all operational aspects of assigned clinical trial(s), including conduct of study start-up, enrollment, study maintenance, and close-out
- Maintains, reviews, and ensures adequacy of information and data contained in applicable tracking tools. (e.g. sites activation & participant enrollment status, reconciliation activities, filing & archiving)
- Assist the Study Lead with the development, oversight, and / or completion of essential clinical documents including, but not limited to clinical study protocol, informed consent form, training slides and materials
- Support site management in overseeing, managing, and tracking performance of participating sites which may include acting as a point of contact as delegated by the manager, facilitating review of site-specific documents, and tracking performance indicators for respective sites.
- Participate in the review of review monitoring / data reports, protocol deviations to ensure reliable quality data is delivered
- Assist with the oversight and maintenance of the study’s TMF
Position Requirements & Experience :
We offer a chance to work with talented people in a collaborative environment. Actual pay will be determined based on experience, qualifications, geographic location, business needs, and other job-related factors permitted by law.
