Clinical Research Associate — Site Monitoring & Compliance
$75 - $85 per hourR & D Partners
R&D Partners is hiring a Clinical Research Associate (CRA) to oversee clinical trial sites in California, United States. The ideal candidate will ensure compliance with protocols and quality standards, provide training to site staff, and support patient recruitment efforts. Key responsibilities include monitoring site performance and maintaining study data accuracy. Strong communication, attention to detail, and knowledge of clinical trial regulations are essential. Compensation ranges from $75 to $85 per hour. #J-18808-Ljbffr R&D Partners
- A renowned clinical research organization in California is looking for a Clinical Research Associate to oversee monitoring activities for clinical sites. Responsibilities include conducting various types of monitoring visits, preparing monitoring reports according to regulatory...WebsiteRemote jobLocal area
$90k - $130k
A leading clinical research organization is seeking a Clinical Research Associate to manage clinical sites and monitor data for trials. The ideal candidate should have at least 2 years of experience in clinical monitoring and a strong understanding of ICH/GCP guidelines...WebsiteRemote job- A clinical research organization is seeking a Clinical Research Associate to conduct site visits for clinical trials in California, Missouri. The role involves ensuring data integrity and protocol compliance while monitoring study sites. Candidates should have a Bachelor...Website
- Overview Experienced Clinical Research Associate - Full-Service Syneos Health is a leading... .... Responsibilities Performs site qualification, site initiation, interim monitoring, site management activities... ...Practice (GPP) and protocol compliance. Uses judgment and experience...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Strategic Solutions is seeking a Sr. Clinical Research Associate for the West Coast to manage clinical trial activities, ensuring compliance with protocols and regulatory... ...requirements. You will be responsible for monitoring trial sites, conducting site visits, and...Website
$30 - $45 per hour
...California Practice/Department: Compliance Work Environment: Field... ...direction of a field supervisor and monitoring environmental sensitive areas... ...all Dudek and construction site safety protocols. Minimum... ...Bachelor’s degree (or in‑progress), Associate’s degree, or commensurate...WebsiteHourly payPart timeWork at officeRemote workLong distance- Mgr, Clinical Operations | Full Service | CRA Line Management + CRA Monitoring Experience Required (Home-Based - US... ...work performed, metric compliance, and development of... ...Clinical Operations on-site performance. Develop... ...plus extensive clinical research experience in a...WebsiteContract workLocal areaWork from homeFlexible hours
- ...(Must Have - Medical Monitoring - Oncology/Protocol Exp... ...accelerate progress.Our Clinical Solutions team members... ...members and clinical site staff; provides... ...therapeutic area. Clinical research experience required.Candidate... ...is committed to compliance with the Americans with...WebsiteContract workWork at officeWorldwideFlexible hours
- IQVIA Argentina is seeking a Clinical Research Associate to provide on-site monitoring and ensure adherence to clinical and regulatory standards. Candidates must have at least 2 years of experience and a Bachelor's degree in a relevant field. The role involves collaborating...Website
- ...with the same molecule. Not all sites are enrolled Monitoring plan allows for flexibility... ..., and close‑out visits for clinical trials. Ensuring protocol compliance, data integrity, and patient... ...monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or...WebsiteFlexible hours
- Overview Responsibilities include monitoring activities for assigned clinical sites, both in person and remote, including planning and execution of visits... .... Experience Requirements > 5 years of experience as a Clinical Research Associate. #J-18808-Ljbffr ProPharmaWebsiteInterim roleWork at officeLocal areaRemote work
- ...CRA to strengthen our clinical operations team in Ventura... ...experience of onsite monitoring activities Profound knowledge of clinical research processes and medical... ...monitoring and site management process Conducting... ...and regulatory compliance and managing required...WebsitePart timeFreelanceLocal areaRemote work
$110.52k - $138.15k
Sr. Clinical Research Associate - West Coast ICON plc is a world‑leading healthcare... ...lead on clinical trial monitoring tasks requiring technical... ...Monitoring clinical trial sites to ensure adherence to study... ...to influence and drive compliance within a complex environment...WebsiteWork experience placementFlexible hours$90k - $130k
..., TX, WA Vanguard Clinical, Inc. is a Contract Research Organization (CRO)... ...Management, Clinical Monitoring, Quality Assurance,... ...of clinical sites and monitoring of clinical... ...Clinical Research Associate (CRA) will execute... ...guidelines to assess compliance with applicable...WebsitePermanent employmentFull timeContract workInterim roleWork at officeRemote workFlexible hours$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - Southern California ICON plc is a world‑leading... ...for performing investigative site management and monitoring activities throughout the clinical... ...site relationships and securing compliance Expertise in GxPs and Oncology monitoring...WebsiteWork experience placementInterim roleLocal areaRemote workFlexible hours$109.5k - $153.3k
...the role As an investigator site facing role, the Sr. CRA will... ...goals. Organize and maintain clinical study documentation (e.g.,... ...for all aspects of study site monitoring including routine monitoring... ...of five (5) years of clinical research monitoring experience (including...WebsiteFor contractorsLocal areaRemote work$71.9k - $189k
Clinical Research Associate, Sponsor Dedicated California, United States of America | Full time | Field-based | R1541733 To be eligible for... ...where the job is located. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close‑out...WebsiteFull timePart timeLocal areaImmediate startWorldwide$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - Southern California ICON plc is a world-leading... ...for performing investigative site management and monitoring activities throughout the clinical... ...site relationships and securing compliance. Expertise in GxPs and Oncology...WebsiteWork experience placementInterim roleLocal areaRemote workFlexible hours- ...an experienced Oncology Sr. CRA 2 in California who will be responsible for all aspects of clinical trial site monitoring. Key responsibilities include ensuring study compliance, managing data integrity, and handling Serious Adverse Event reports. The ideal candidate will...WebsiteNight shift
- ...details about this job. Air Pollution Monitoring Technical Support This position is a 12-... ...These include mobile laboratories, fixed-site monitoring, and distributed sensor networks... ...work alongside another SAPS and two Associate Governmental Program Analysts (AGPAs) dedicated...WebsitePermanent employmentFor contractorsWork at officeLocal areaRemote workTrial periodNight shift
$105k - $117k
...based in California, Missouri, or other major hub locations across the US. The role involves site monitoring, ensuring protocol adherence, and managing data integrity in clinical trials. Candidates need a degree in a related health profession and 1-3 years of clinical...Website$110.52k - $138.15k
ICON Strategic Solutions is looking for a Senior Clinical Research Associate to manage oncology clinical trials in Southern California. Responsibilities include site management, monitoring, and ensuring data integrity and subject safety. Candidates should have at least...Website$18 - $34 per hour
...qualified, experienced Cultural Resource Monitors for a high-profile transportation... ...lead monitors to ensure punctuality, on-site safety, and cultural resource protection... ...project teams. Dudek is also committed to compliance with all applicable laws providing equal...WebsiteHourly payDaily paidPart timeWork at officeRemote workLong distance$19.02 - $20.02 per hour
...benefits. Job Summary and Purpose The Monitor is the entry level position that... ...; maintain records of client compliance of program rules, report to clinical/case management staff, assist clinical... ...as human service locations, work sites, and medical facilities Assists...WebsiteHourly payWork at officeLocal area- ...application process. Client Service Monitor - FT Day shift Full Time... ...(CSM) works directly on‑site and is responsible for keeping... ...to promote safety and program compliance Conducts routine site walk‑throughs... ...unpleasant sensory demands associated with the participants’ use of...WebsiteFull timeContract workInterim roleWork at officeLocal areaFlexible hoursShift workNight shiftDay shift
$21.5 - $22.5 per hour
Client Services Monitor - DMH Van Nuys Full Time Manual Labor Van... ...for the upcoming DMH Van Nuys site Location: 6909 Sepulveda Blvd... ...client supervision Ensure client compliance with program rules, policies,... ...unpleasant sensory demands associated with the clients use of...WebsiteHourly payFull timeInterim roleWork at officeLocal areaNight shiftWeekend workDay shift- ICON is seeking a Senior Clinical Research Associate - Oncology in California. This role focuses on site management and monitoring for oncology clinical trials. The ideal candidate has a Bachelor's degree, over 5 years of experience in monitoring clinical trials, and expertise...Website
- Superintendent - Operations, Monitoring, and Maintenance (OM&M) At Essel, we lead the way in... ...team, overseeing daily landfill site activities, ensuring project alignment with... ...interpret plans and schematics, and ensure compliance with codes and regulations. Health and...WebsiteLocal area
- ...Resource Management is looking for an on-call archaeologist based in California. This role involves fieldwork, conducting surveys, and site testing while ensuring that work is carried out according to established standards. Candidates should have a bachelor's degree in...Website
$25 - $33 per hour
...Resource Management is hiring an on-call Archaeologist in California. The role entails conducting field surveys, monitoring site testing, and ensuring compliance with safety protocols. Candidates should have a degree in Archaeology or a related field, strong analytical...WebsiteHourly payPart time
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