Clinical Research Coordinator - Study Operations & Compliance
UCLA Health
UCLA Health in Santa Monica, CA is seeking a Clinical Research Coordinator to support management of clinical research activities across the study lifecycle, from design to closeout. You will implement and manage activities for one or more studies, prioritizing tasks to meet deadlines and ensure compliance with study protocols, CFR, and ICH-GCP. You will collaborate with the Principal Investigator, ancillary departments, sponsors, and external sites to support compliant study conduct, financial #J-18808-Ljbffr UCLA Health
- ...Health in Los Angeles, CA is seeking an Assistant Clinical Research Coordinator to manage and coordinate clinical research activities across one or more studies. You will ensure protocol adherence, regulatory compliance, and collaboration with the PI and multidisciplinary...Operations
- ...: Collects data for clinical trials research, independently. Prepares... ...the submission of study documentation to... ...activities and research lab operations. Completes timely... ...applications in compliance and consistency with... ...clinical sites, and data coordinating centers as...OperationsFor contractorsFor subcontractorLocal area
$33 - $40 per hour
...Valley, and Whittier clinics Schedule: Monday-Friday... ...Job Title: Clinical Research Coordinator (Oncology) Job... ...patient participation and study conduct. This role focuses... ...documentation and compliance with study protocols.... ...ensure smooth study operations. + Follow all site...OperationsFull timeContract workTemporary workPart timeLocal areaMonday to Friday- ...Assistant Clinical Research Coordinator The Assistant Clinical Research Coordinator... ...of clinical research studies within a healthcare setting... ...clinical trials are conducted in compliance with study protocols,... ...Adhere to site standard operating procedures (SOPs) and Good...OperationsWork at officeMonday to Friday
$71k - $91.85k
...Collects data for clinical trials research, independently. Prepares... ...the submission of study documentation to regulatory... ...and research lab operations. Completes timely... ...applications in compliance and consistency with... ...clinical sites, and data coordinating centers as...OperationsFull timeTemporary workFor contractorsWork experience placementFor subcontractorLocal areaFlexible hoursShift 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...
- Folio Clinical Research in Los Angeles, CA is seeking a Lead Clinical Research Coordinator to manage trial activities under the Principal Investigator. You will coordinate daily operations, ensure regulatory compliance, and support informed consent and participant communication...Operations
$25 - $32 per hour
...alternative application process. Clinical Research Coordinator I FullTime Technical West... ...trials by coordinating study visits, managing data collection, and ensuring compliance with protocols and regulatory... .... Adhere to site standard operating procedures (SOPs)....Hourly payFull timeH1bMonday to Friday- Description Clinical Trial Manager - Full Service... .../GCP/regulatory compliance and data... ...RACT). Reviews the study scope of work, budget... ...experience, operational data, metrics and... ...Data Management to coordinate delivery handoffs... ...conduct of a clinical research project....OperationsContract workTemporary workImmediate startFlexible hours
- ...Senior Clinical Research Coordinator Overview Full-time / Direct-hire On-site Essential... ...Site Director to ensure compliance and productivity of all clinical site staff and operations. Manage, train and support... ...comprehend and communicate study protocols. Oversee Site Initiation...OperationsFull timeInterim role
- ...Clinical Research Coordinator IIReports to: Research Regulatory/QC ManagerLocation... ...independently manages the full study lifecycle—from feasibility... ...records per regulatory/compliance standards at all times... ...owns day-to-day research operations for the site with minimal...OperationsWork at officeFlexible hoursNight shift
- ECN Operating LLC in California seeks a Travel Clinical Research Coordinator to support site openings, patient recruitment, enrollment, and startup tasks across study sites while ensuring compliance with GCP and study protocols. Travel up to 75% is required; the role collaborates...
- ...COMPANY OVERVIEW Alliance Clinical Network we're people with a... ...technology through groundbreaking research. We bring our energy and... ...of clinical trials in compliance with study protocols, regulatory guidelines... ...criteria. Schedule and coordinate participant visits, including...Work at officeMonday to Friday
- ...the Role: National Clinical Trials Inc. is looking... ...detail-oriented Clinical Research Coordinator II (CRC II) to join our... ...and manage day-to-day operations of clinical trials in compliance with FDA regulations, GCP... ..., and follow up with study participants while ensuring...Operations
$62.4k - $83.2k
...Clinical Research Coordinator Inglewood Clinical is part of the Irvine Clinical Research... ..., patient safety, and operational excellence. Job Duties Study Management: Serve as the primary... ...initiation to closeout. Protocol Compliance: Execute study procedures with...OperationsHourly payFull time- Inglewood Clinical is part of the Irvine Clinical Research site network, the largest... ...Clinical Research Coordinator We are seeking a dedicated... ...Oakland location. Study Management: Serve... ...day-to-day operations from site initiation... .... Protocol Compliance: Execute study procedures...Operations
- Clinical Research Coordinator Phlebotomy Trained Lightship is a clinical trial site organization delivering... ...communities. Our investigators and study teams follow participants across all... ...IEC requirements, Lightship Standard Operating Procedures (SOPs), and applicable site...OperationsContract workInterim roleWork at officeWeekend workAfternoon shift
$65k - $85k
...alternative application process. Lead Clinical Research Coordinator - Los Angeles, CA Full Time... ...trial activities, ensuring compliance, quality, and efficiency... ...managing clinical research operations, from feasibility assessments to study close-out. Operational Expertise...OperationsFull timeContract workInterim role$33.09 - $65.77 per hour
...Clinical Trials Project ManagerWork Location: Los Angeles, CAJob #... ...as part of a groundbreaking Research team, working to understand hundreds... ...to protocol development, study start?up, and regulatory... ...adaptability to ensure smooth trial operations and support high?quality...OperationsMonday to FridayShift work- ECN Operating LLC in Los Angeles, CA seeks a Clinical Research Coordinator to manage and support all aspects of clinical trials, including recruitment, data collection, regulatory compliance, and specimen handling. Bachelor's in a health-related field is required; 1-2...
- National Clinical Trials Inc. is seeking a detail-oriented Clinical Research Coordinator II (CRC II) to join our team in Los Angeles, CA. You will coordinate and manage clinical trials, ensuring FDA/GCP/ICH compliance, and serve as the main liaison with sponsors and IRB...
- Cedars-Sinai in Los Angeles is seeking a Clinical Research Coordinator II to support the Endocrinology Division in the Department of Medicine. You... ...data collection, and reporting while ensuring regulatory compliance and high-quality documentation. Responsibilities include...
- Irvine Clinical Research is seeking a dedicated Clinical Research Coordinator for our West Coast network. The successful candidate will manage Phase II/III trials, ensure... ..., and uphold patient safety across site operations. Ideal applicants have 2-4+ years of trial coordination...Operations
- ...Job Description Job Title: Clinical Research Coordinator Location: Inglewood, California... ...and execution of clinical research studies, ensuring compliance with all regulatory guidelines. This... ...procedures to ensure smooth operations. This is an onsite, contract opportunity...OperationsContract workWork at officeLocal area
$82.71k - $133.07k
...Senior Clinical Research Coordinator Work Location: Santa Monica, CA, USA Onsite... ...critical role in the overall operational management of clinical research/trial/study activities from design, set... ...on the administration of the compliance, financial, personnel and...Local areaRemote workMonday to FridayFlexible hours- ...Career Opportunities with ECN Operating LLC A great place to work.... ...organized and motivated Clinical Research Coordinator (CRC) to join our research... ...trials and research studies, including subject recruitment... ...data collection, regulatory compliance, and specimen handling....Work at office
$263.76k - $356.85k
...the lives of patients as we research, manufacture, and deliver innovative... ...Director, Global Site Study Operations, AmericasWhat you will doLet... ...across the Americas clinical trial portfolio. This role provides... ..., high-quality delivery in compliance with ICH-GCP, regulatory requirements...OperationsFull timeLocal areaRemote workFlexible hours- ...Description EXPERIENCED Clinical Research Coordinator - Onsite Job Details... ...on the start date of new studies and enrollment in current... ...CRO’s. The CRC maintains compliance with all regulatory bodies... .... Comply with standard operating procedures of the sponsor,...Full timeWork at officeLocal areaRemote workVisa sponsorship
$38.19 - $61.45 per hour
...toggle section visibility Under the direct supervision of the Clinical Trials Administrator, the Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, setup, conduct, through closeout. The...Hourly payFull timeLocal areaMonday to FridayFlexible hours$82.71k - $133.07k
...keys to toggle section visibility Job Qualifications Required: Bachelor's Degree or three-to seven years of study coordination or clinical research coordination experience Ability to work efficiently and complete tasks with a high degree of accuracy....Remote workMonday to FridayFlexible hours
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