Clinical Research Coordinator: Study Ops & Participant Support
Medix™
Medix is seeking a detail-oriented Clinical Research Assistant in Los Angeles to support the coordination and execution of clinical research protocols under the supervision of the PI and senior staff. You will assist with informed consent and enrollment, educate participants, monitor study progress, and report adverse events and protocol deviations. You will also uphold SOPs and GCP guidelines, keep organized records, and work collaboratively to resolve questions in a fast-paced environment. #J-18808-Ljbffr Medix™
- Kelly Services is seeking a Clinical Research Coordinator for a 5-month temporary position at a clinical... ...in West Hills, CA. This role supports study visits, data management, and regulatory... ...visits, screening and enrolling participants, maintaining records, and collaborating...SuggestedTemporary work
- ...of California - Los Angeles Health is seeking an Assistant Clinical Research Coordinator to support the Principal Investigator in daily operations of Neurology clinical studies. You will recruit participants, assist with informed consent, review medical charts, administer...Suggested
- Adventist Health Glendale is seeking a Clinical Research Coordinator to coordinate and participate in clinical studies under the guidance of principal investigators, ensuring... ...charts and tests, prepare reports, and support regulatory submissions while supervising a small...Suggested
- Cedars-Sinai seeks a Clinical Research Coordinator I to independently coordinate studies in the Surgery Chair Department. You will screen patients for eligibility,... ...accurate data collection and CRF documentation, and support sponsor queries while maintaining regulatory...Suggested
$28 - $30 per hour
Description Clinical Research Coordinator Kelly® Science & Clinical is seeking a Clinical Research Coordinator... ...and execute clinical research studies by screening and enrolling participants, collecting and managing data, supporting study visits and procedures, maintaining...SuggestedTemporary workLocal areaMonday to Friday- ...Clinical Trial Manager - Full Service Syneos... ...and progression; supportive and engaged line... ...RACT). Reviews the study scope of work,... ...risk mitigations. Participates and presents in key... ...Management to coordinate delivery handoffs... ...conduct of a clinical research project....Contract workRemote workFlexible hours
$120k - $135k
...Clinical Project Manager - Oncology (Client... ...and progression; supportive and engaged line... ...advancing cancer research and bringing innovative... ...of oncology studies across multiple indications... ...providers Coordinate Clinical Trial... ..., eligibility to participate in Employee Stock...Contract workWork at officeRemote workWorldwideFlexible hours- ...Summary: Collects data for clinical trials research, independently. Prepares and/or supports the submission of study documentation to... ...of research staff and/or participants on protocols, documentation... ...clinical sites, and data coordinating centers as applicable; and...For contractorsFor subcontractorLocal area
- ...Statement/Position Summary: The Clinical Research Coordinator I assists Principal Investigators and other study team members in the... .... Responsibilities include supporting clinical trials involving CAR... ...conducting follow-up with enrolled participants to ensure protocol...Work experience placementMonday to Friday
$43 - $53 per hour
...START Center for Cancer Research ("START") is the... ...currently hiring a Clinical Research Coordinator. The Clinical Research... ...research staff to support the daily activities... ...coordinating patient participation in the trial. The... ...regular basis with Study Sponsor's, CRO's, staff...Hourly payCurrently hiringWork at officeLocal areaWorldwideMonday to FridayFlexible hours$72.86k - $97.14k
...Clinical Research Coordinator II Locations: Los Angeles, California Job Category:... ...clinical trials across all phases of study protocols for the Transplant and... ...and research team members, supporting study start-up, participant recruitment and enrollment, data...Full timeWork experience placementLocal areaMonday to FridayShift work- Cedars-Sinai in Beverly Hills, CA seeks a Clinical Research Coordinator II to lead logistics for multiple studies, ensuring protocol compliance and patient safety. You will interact with investigators, staff, and sponsors to execute trials and manage data collection. The...
- ...Clinical Research Coordinator The Department of Surgery is seeking an experienced... ...Research Coordinator to support interventional clinical trials... ...coordinating and managing study activities for both drug... ...device trials, including participant recruitment, study...Hourly payFlexible hours
- ...Description EXPERIENCED Clinical Research Coordinator - Onsite Job Details... ...on the start date of new studies and enrollment in current... ...clinical trials. The CRC supports multiple Phase II-IV clinical... ...to identify eligible participants for clinical trials. Educates...Full timeWork at officeLocal areaRemote workVisa sponsorship
$30 - $40 per hour
...Description Inglewood Clinical is part of the Irvine Clinical Research site network, the largest... ...Clinical Research Coordinator to drive trial success... ...excellence. Job Duties Study Management: Serve as... ...Coordination: Guide participants through complex visit schedules...Hourly payFull time$30.74 - $49.46 per hour
...Description The Assistant Clinical Research Coordinator (ACRC) contributes to... ...clinical research/trial/study activities from design,... ...necessary deadlines. The ACRC participates in planning and organizing... ...entities as needed to support the administration of...Hourly payLocal areaFlexible hours$28 - $30 per hour
...Description Kelly® Science & Clinical is seeking a Clinical Research Coordinator for a contract-to-hire... ...Coordinators to support the successful execution... ...and execution of vaccine study protocols under the supervision... ...Schedule and facilitate participant study visits, procedures...Contract workTemporary workWork at officeLocal areaImmediate start$27 per hour
...Inglewood Clinical is part of the Irvine Clinical Research site network, the largest of its kind... ...a Clinical Research Coordinator I to drive trial success... ...of a clinical research study Perform study... ...screen potential study participants Conduct diagnostic,...Full time- ...groundbreaking biomedical research facilities and world-... ...innovation and supports the gold standard of... ...in this role? The Clinical Research Coordinator I works independently providing study coordination, screening... ...concepts and details, and participating in the informed...Full timeLocal area
- ...Adventist Health Glendale is proud to be part of the thriving, diverse community since 1905. Job Summary: Coordinates and participate in clinical research studies conducted by principal investigator(s). Coordinates and participate in a variety of complex activities...Daily paidFull timeWork experience placementDay shift
- ...you a passionate and dedicated research professional? Cedars-Sinai'... ...second opinions. The Clinical Research Coordinator I works independently providing study coordination, screening of potential... ...concepts and details, and participating in the informed consent...Full timeWork at officeLocal areaShift work
- ...Department of Surgery is seeking an experienced Clinical Research Coordinator to support interventional clinical trials across... ...for coordinating and managing study activities for both drug and device trials, including participant recruitment, study implementation, data...Hourly payFull time
- ...you must reside in the commutable area. The Clinical Research Coordinator III works independently providing study coordination including screening of potential... ...presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible...Full timeLocal area
- Irvine Clinical Research - West Los Angeles / Inglewood location seeks a Clinical Research Coordinator I to manage day-to-day trial operations, coordinate... ...clinical team to recruit participants, conduct assessments, and maintain accurate study documentation in a fast-...Full time
- ...data collection for clinical trials research. Prepares, submits and... ...compilation of study documentation is sent... ...review and approval. May support clinical trials... ...research staff and/or participants on protocols, documentation... ...sites, and data coordinating centers as...Temporary workFor contractorsFor subcontractorLocal area
- ...About the Role: National Clinical Trials Inc. is looking for... ...detail-oriented Clinical Research Coordinator II (CRC II) to join our... ...enroll, and follow up with study participants while ensuring protocol adherence... ...clinical teams Support site initiation visits, monitoring...
$71k - $91.85k
...Summary: Collects data for clinical trials research, independently. Prepares and/or supports the submission of study documentation to... ...of research staff and/or participants on protocols, documentation... ...clinical sites, and data coordinating centers as applicable; and...Full timeTemporary workFor contractorsWork experience placementFor subcontractorLocal areaFlexible hoursShift work- ...Job Description Job Description Clinical Research Coordinator (CRC) preferably with oncology experience... ...coordinator for all assigned studies and backup for other coordinators.... ...with study requirements for patients participating in clinical trials. Collaborates...Temporary workLocal areaFlexible hours
- The START Center for Cancer Research in Los Angeles, CA is hiring a Clinical Research Coordinator to support early phase oncology trials... ...ensure accurate conduct of studies, adherence to protocols and... ..., coordinate patient participation, and help maintain regulatory...
- The START Center for Cancer Research is hiring a Clinical Research Coordinator to support daily activities of early phase oncology trials... ...You will ensure accurate conduct of studies, adherence to GCP, and safe patient participation with supervision from senior staff. Typical...Monday to Friday
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