- Stanford University (Stanford, CA)
- …database queries as required. + Collect, process and ship specimens in accordance with clinical protocol and IRB. + Assemble study kits for study visits and ... Clinical Research Coordinator Associate **School of...CRCA will manage data, enroll and follow patients on trial and assist with regulatory and financial requirements of… more
- Actalent (San Francisco, CA)
- …with experience in clinical research to support an ongoing Infectious Disease clinical trial . The ideal candidate will be able to work independently. Key ... Part-Time Clinical Research Coordinator Contract Duration: Until...to Detail: High level of accuracy in documentation and protocol compliance. Job Type & Location This is a… more
- System One (Boston, MA)
- …Bachelor's Degree Requirements: 1-3 years of relevant experience in human clinical trial research, with cardiovascular disease experience preferred Knowledge ... Title: Drug Clinical Research Coordinator Location: Boston MA...and Trial Close-out Assist in development of trial protocol IRB application and submit to… more
- UCLA Health (Los Angeles, CA)
- …Research Coordinator contributes to the overall operational management of clinical research/ trial /study activities from design, set up, conduct, through ... organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and...and ICH Good Clinical Practice (GCP). The Clinical Research Coordinator collaborates with the Principal… more
- UCLA Health (Santa Monica, CA)
- Description The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/ trial /study ... and prioritizes work to reach scheduled goals. The Senior Clinical Research Coordinator is a technical leader...is a technical leader responsible for ensuring the study protocol and procedures have been completed accurately, safely, and… more
- Alabama Oncology (Birmingham, AL)
- Description of Duties: * Screens all potential patients for protocol eligibility. Maintains and submits monthly screening logs. * Presents trial concepts and ... patient's scheduling for tests and treatments required by the protocol . * Documents any changes in the patient's condition,...and transports the study drug to the pharmacy or clinical team for distribution to the patient at the… more
- Caris Life Sciences (Phoenix, AZ)
- …+ Candidates should have 1-2 years' experience in a Biorepository setting or Clinical Trial setting + Proficient in Microsoft Office Suite, specifically Word, ... biological science + 3-5 years' experience + Candidates should have experience with clinical trial regulatory documentation or TMF. + Candidates should have a… more
- Baylor Scott & White Health (Dallas, TX)
- …executes a variety of different project workflows based on the needs of the clinical trial protocol . Examples of workflows include, providing in-service ... **JOB SUMMARY** The Clinical Research Coordinator 1 assists various...preparing Institutional Review Board (IRB) materials for approval of protocol amendments and submitting Investigational New Drug (IND) Safety… more
- Children's Hospital Boston (Boston, MA)
- …independently carries out studies. Responsible for screening patients for trial participation, enrolling patients, monitoring protocol implementation, completing ... of the study. Implements processes and procedures to meet study goals and protocol requirements. May participate in training Clinical Research Assistants and… more
- Stanford University (Stanford, CA)
- Assistant Clinical Research Coordinator (1 year fixed term/80% FTE) On-site **School of Medicine, Stanford, California, United States** Research Post Date Nov ... by Dr. Garry Gold is seeking an 80% FTE Clinical Research Coordinator to work in person...Perform basic measurements and tests on patients according to protocol , such as collecting saliva specimens. + Order and… more