Freelance Part-Time Clinical Research Associate - Site Monitoring
SanaClis
A global clinical research organization is seeking a part-time Freelance Clinical Research Associate (CRA) to join their team. The role involves monitoring clinical trials, ensuring compliance with regulations, and maintaining data integrity. The ideal candidate should have a Bachelor’s degree in life sciences or related fields, with at least 2 years of relevant experience. English proficiency at C1 level is required, and a valid driving license with travel capability is essential. Enjoy a balanced work-life environment and growth opportunities. #J-18808-Ljbffr SanaClis
- ...We are looking for a FREELANCE, PART-TIME CRA to strengthen our clinical operations team in Ventura,... ...of experience of onsite monitoring activities Profound knowledge of clinical research processes and medical terminology... ...clinical monitoring and site management process...Part timeFreelanceWebsiteLocal areaRemote work
$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 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
- AbbVie seeks a Clinical Research Associate to support investigative sites and coordinate trial execution. You will ensure protocol... ...integrity, patient safety, and timely communications with site staff... ...You will conduct site training, monitor risk, and collaborate with the...Website
- Parexel International is seeking a Senior Clinical Research Associate (Sr. CRA) to manage investigator sites across trials, ensuring patient safety and trial quality... ...and sponsor standards. The role emphasizes site monitoring from activation to database lock, interaction...Website
$80k
...Position Overview Premier Research is looking for a CRA II, Onc/Neuro... ..., Northeast) to join our Clinical Monitoring and Site Management team. As a Clinical Research Associate II, you will conduct all monitoring... ..., patient safety, and timely deliverables. Ensure validity...WebsiteFull timeWork experience placementInterim roleLocal areaRemote work- ...Clinical Research Associate – Full-Service Syneos Health is a fully integrated biopharmaceutical... ...Job Responsibilities Perform site qualification, site initiation, interim monitoring, site management activities... ...to travel up to 75% of the time. U.S. only: deployment may...WebsiteInterim roleLocal areaImmediate startRemote workFlexible hours
- ...Description Clinical Research Associate - Full-Service Syneos Health® is... ...Responsibilities Performs site qualification, site initiation, interim monitoring, site management... ...regular basis US ONLY: As part of your employment... ...performance, and flexible paid time off (PTO) and sick...WebsiteContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- Rho is seeking a Clinical Research Associate II or Senior CRA to monitor pain studies and manage site visits. You will ensure protocol adherence, maintain regulatory compliance, and coordinate trial documentation. The role requires 8-10 site visits per month with travel...WebsiteRemote job
- EPM Scientific, San Francisco, CA, seeks a Clinical Research Associate (Sr.) for a hybrid role at our local SF site. You will manage and investigate trials, coordinate monitoring, and travel 20-25% to sites as needed. Ideal candidate has 2+ years onsite monitoring with...WebsiteLocal area
- Sonova is seeking a Clinical Research Associate (Remote) to support global medical device clinical studies... ...coordination with investigative sites, cross-functional teams, and regulatory... ...experience (1+ year with site monitoring), and proficiency with CTMS/EDC/eTMF,...WebsiteRemote job
- Vanguard Clinical, Inc. is seeking a Senior Clinical Research Associate (Sr. CRA) to manage clinical sites and monitor data across Phases 1-3 in accordance with ICH/GCP and SOPs. This role reports to the Director, Clinical Monitoring and requires travel up to 75% globally...WebsiteRemote job
- ...standard of care for participants in clinical trials and respond to emergency... ...situations based upon clinical research standards Perform all aspects of study site monitoring, including routine monitoring... ...to travel overnight 60% of the time Comfortable working in a fast-...WebsiteLocal areaNight shift
$100k - $125k
Clinical Research Associate (Sr.) - EPM Scientific, San Francisco County, CA. MUST... ...role at their San Francisco site. Their commercial supply of... ...aspects of clinical monitoring and site management 20-25%... ...early in your career Being a part of team whose work directly...WebsiteLocal area$100k - $112k
...California or Colorado with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and... ...utilize your skills, knowledge, and clinical judgement to provide a high standard... ...emergency situations based upon clinical research standards. Responsibilities...WebsiteWork at officeLocal areaRemote workNight shift- The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good...WebsiteLocal areaRemote work
$110.52k - $138.15k
Senior Clinical Research Associate - Oncology (Myelofibrosis) - West Region... ...investigational sites and the sponsor Conduct... ...initiation, routine monitoring, and close‑out... ...patient safety, ensuring timely and accurate AE/SAE/PQC... ...for any part of the application process...WebsiteWork experience placementLocal areaVisa sponsorshipFlexible hours$90k - $140k
...who take healthcare and clinical research personally, with... ...hiring a Clinical Research Associate II or Senior Clinical... ...Associate in experience in monitoring pain studies to join... ...monitoring and site management process in... ...are eligible for paid time off, holidays, parental...WebsiteHourly payCurrently hiringLocal areaRemote work- Fortrea is seeking a CRA 2 in California or Colorado with 2 years of monitoring experience. This role requires 8-10 days on site per month, blending onsite and remote work to support clinical trial monitoring. You will conduct site visits, ensure protocol compliance, manage...WebsiteRemote job
$120k - $145k
...interest from both full-time employees and... ...TN, TX, WA Vanguard Clinical, Inc. is a Contract Research Organization (CRO) headquartered... ...Director, Clinical Monitoring, primarily... ...management of clinical sites and monitoring of... ...Senior Clinical Research Associate (Sr. CRA) will...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... ...responsible for performing investigative site management and monitoring activities throughout the clinical... ...reasonable accommodation for any part of the application process, or in...WebsiteWork experience placementInterim roleLocal areaRemote workFlexible hours$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- Premier Research is seeking a CRA II, Onc/Neuro/Rare/Derm (West Coast, Midwest, Northeast) to join our Clinical Monitoring and Site Management team. You will conduct monitoring visits, manage data integrity, maintain eTMF, and support study sites throughout the project...Website
- Ergomed Group is seeking a monitoring professional to support on-site or remote visits across phase 2/3 trials, ensuring sites remain suitable for study conduct. You will verify investigators' qualifications, train site staff, and assist with regulatory submissions; travel...WebsiteRemote jobWorldwide
- ...Summary Job Description The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical... ...professional responsible for managing site monitoring and relationship activities across... ...strong presentation, organizational, time‑management, and prioritization...WebsiteHourly payContract workRemote workWorldwideShift work
- Jobtailor is seeking a Local Project Coordinator to oversee clinical monitoring and study site management in the United States. You will ensure regulatory compliance, data integrity, and proper training for site staff while coordinating with vendors and sponsors. The role...WebsiteLocal areaNight 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- ...-care community hospital in Sherman Oaks, California seeking a Monitor Tech. You will monitor cardiac rhythms, assist nursing staff, and... ...Certificate within 30 days, and current BLS certification. Part-time night shifts are offered with a comprehensive total rewards package...Part timeNight shift
- Syneos Health/ inVentiv Health Commercial LLC is hiring a Clinical Research Associate in California. This role includes performing site qualification, monitoring, and management activities while ensuring compliance with regulatory standards. The ideal candidate holds a...WebsiteFlexible hours
- ...Palo Alto, California, is seeking a Cardiology Technician I to conduct and record electrocardiograms (ECG) and attach ambulatory monitors under supervision. The role includes patient instruction, data file maintenance, and assisting in staff training. You will ensure...Part time
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