Clinical Research Coordinator Jobs in Venice, CA
Thinkbyte Consulting inc
West Los Angeles, CA
The Clinical Research Coordinator (CRC) – Oncology is responsible for the coordination and implementation of oncology-focused clinical research studies. The CRC ensures that studies are conducted in accordance with local, state, and federal regulations and institutional policies, with an emphasis on participant safety and protocol fidelity.
National Medical Association
Santa Monica, CA
The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Mathematical skills sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
CEDARS-SINAI
$23.39 - $39.76 HOUR
Beverly Hills, CA
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Primary Duties and ResponsibilitiesIndependent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
CEDARS-SINAI
$23.39 - $39.76 HOUR
Beverly Hills, CA
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. In collaboration with the physician and other medical personnel, documents thoroughly on Case Report Forms (CRFs) the following; changes in patient condition, adverse events, concomitant medication use, protocol compliance, response to study drug.
CEDARS-SINAI
$23.39 - $39.76 HOUR
Beverly Hills, CA
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. This exciting opportunity at a top medical center involves cutting-edge cancer research and requires strong skills in data entry, planning and scheduling, and computer literacy to support a dynamic and collaborative team.
CEDARS-SINAI
$28.3 - $48.11 HOUR
LOS ANGELES, CA
The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Primary Duties and ResponsibilitiesIndependent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
CEDARS-SINAI
$23.39 - $39.76 HOUR
Los Angeles, CA
The Clinical Research Coordinator I will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff.
CEDARS-SINAI
$30.84 - $47.8 HOUR
Los Angeles, CA
The Angeles Clinic & Research Institute has established an international reputation for developing new cancer therapies, providing the best in experimental and traditional treatments, and expertly guiding and training the next generation of clinicians. Establishes and completes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety.
Care Access
Los Angeles, CA
Due to enhanced experience in Care Access’ decentralized clinical research process, the Travel Clinical Research Coordinator will be able to assume a greater study workload, overall study responsibility, and more detailed interactions with Site, Sponsor, and CRO, while conveying a positive image of Care Access Research to the community, Sponsors, CROs, and study participants and their family members. Based out of the San Diego-Los Angeles area, the Travel Clinical Research Coordinator's primary responsibilities are to utilize Good Clinical Practices (GCP) in the process of screening, enrolling, and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
CEDARS-SINAI
$23.39 - $39.76 HOUR
Los Angeles, CA
The Clinical Research Coordinator I will work independently providing study coordination, screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff.
CEDARS-SINAI
$26.64 - $41.29 HOUR
Los Angeles, CA
Primary Duties & ResponsibilitiesPerform accurate processing of research laboratory specimens while demonstrating a moderate degree of proficiency and understanding of research protocol and laboratory procedures, including centrifuging, aliquoting, storing, and shipping of specimens. This individual will interact with principal investigators, subjects, clinic and research staff, laboratory staff, medical professionals, pharmaceutical staff, and Sponsor representatives to successfully implement research protocols, in compliance with all regulatory requirements.
CEDARS-SINAI
$23.39 - $39.76 HOUR
Los Angeles, CA
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff.
PRIDE Health
$1961 WEEK
Los Angeles, CA
PRIDE Health is the minority-owned healthcare recruitment division of Pride Global—an integrated human capital solutions and advisory firm. Pay package is based on 8 hour shifts and 40.0 hours per week (subject to confirmation) with tax-free stipend amount to be determined.
CEDARS-SINAI
$28.3 - $48.11 HOUR
Los Angeles, CA
The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Additionally, applicants should bring strong data analysis and management skills, ideally with experience working with clinical or digital health data, statistical software (e.g., R, Stata, SAS), and tools like REDCap.
CEDARS-SINAI
$58864 - $100068.8 YEAR
Los Angeles, CA
The Clinical Research Coordinator II works independently providing study coordination including screening of patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff.
CEDARS-SINAI
$23.39 - $39.76 HOUR
Los Angeles, CA
The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Primary Duties and ResponsibilitiesIndependent study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details to the patients, and participating in the informed consent process.
CEDARS-SINAI
$71219.2 - $121076.8 YEAR
Los Angeles, CA
The Clinical Research Coordinator III works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Cedars-Sinai is one of the largest nonprofit academic medical centers in the U.S., with 886 licensed beds, 2,100 physicians, 2,800 nurses and thousands of other healthcare professionals and staff.
TANNER & ASSOC INC
Los Angeles, CA
Provide initial clinical designs for future trials, partnering with research, translational oncology, biostatistics, clinical operations, regulatory, and pharmacology for input/alignment and presentation at Therapeutic Development Team meetings. Medical monitoring of Phase I-III trials, serving as the primary Clinical Science contact on the Protocol Execution Teams and the primary liaison for clinical operations and Medical Monitor inquiries from sites, monitors, and CROs.