Clinical Research Associate: Site Monitor & Data Integrity
allied executive solutions
Allied Executive Solutions is seeking a Clinical Research Associate to monitor trial sites, ensuring adherence to protocol, SOPs, and GCP. You’ll serve as the primary contact between sponsors and investigative sites to safeguard data integrity and participant safety. The role covers site visits, SDV/SDR, data reconciliation, and TMF maintenance, with opportunities for travel and professional growth in a dynamic research environment. #J-18808-Ljbffr
- ...ICON Strategic Solutions is seeking a Clinical Research Associate with oncology monitoring experience to join our sponsor-dedicated team. You will conduct site visits, ensure protocol and data integrity, and collaborate with investigators to drive study success across...DataWebsite
- ...Health, Inc. is seeking an Experienced Clinical Research Associate aligned across the US. The role focuses on site qualification, initiation, monitoring, and close-out activities, ensuring ICH-GCP compliance and reliable data integrity. Candidates should have a...DataWebsiteRemote work
- ...Syneos Health, Inc. is seeking a Clinical Research Associate for remote work supporting US sites. You will perform site qualification, initiation, monitoring, and close-out visits, on-site or remotely... ...ICH-GCP compliance and accurate data collection. The role requires...DataWebsiteRemote work
- Abbott is seeking a Clinical Research Associate (CRA) to support sites from start-up through closeout. The role requires working in a regulated... ...Teams and Operations. The candidate will monitor sites for protocol compliance, data quality, and GCP, while managing timelines...DataWebsiteRemote job
- ...Syneos Health is hiring a Sponsor Dedicated CRA I/II to support clinical monitoring activities across sites, ensuring regulatory compliance and data integrity. You will perform site visits, review ISF/TMF, and help prepare for audits in a Real World Late Phase setting...DataWebsiteRemote work
- ...IQVIA is seeking a site-monitoring professional to ensure sites conduct studies per protocol and regulatory requirements. The role emphasizes site management, data integrity, and communication with study teams. Responsibilities include monitoring visits, overseeing recruitment...DataWebsite
$60 - $76 per hour
...Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed to accelerating... ...uncompromising data quality, safety, and... ...innovation and integrity If you’re passionate about... ...Time Psychedelic Dosing Monitor / Therapist to support...DataWebsiteHourly payPart timeRemote work3 days per week$74.5k - $197.5k
...is located.Perform monitoring and site management work to ensure... ...and reporting study data as required by the... ...of work and Good Clinical Practice.• Work with... ...Evaluate the quality and integrity of study site... ...experience as a Clinical Research Associate (CRA) in a CRO,...DataWebsiteFull timePart timeLocal areaImmediate startWorldwide$103k - $130k
...translational research. We’re bringing... ...labs to mobile clinics. By helping providers... ...Research Associate (Sr. CRA) is responsible... ..., execution, monitoring and close-out... ...research sites and/or laboratories... ...timely data collection and... ...execution, data integrity and adherence to...DataWebsiteHourly payFull timeContract workRemote workWork from homeWorldwideFlexible hoursNight shift- ...Placements24 is seeking a dedicated Clinical Research Associate to oversee Phase III trials... ...between sponsors and investigative sites, ensuring data integrity, compliance with GCP, and regulatory... ...include site initiation, monitoring, and close-out visits, data verification...DataWebsite
- ...Placements24 is seeking a diligent Clinical Research Associate to join a globally distributed team in a fully remote role. You will monitor sites, ensure adherence to protocols, and maintain data integrity across trials from your home office. The ideal candidate holds...DataWebsiteRemote workHome office
- ...Worldwide Clinical Trials in the United States seeks a Clinical Research Associate to support site qualification, monitoring, and study close-out visits across diverse therapeutic areas... ...site staff to ensure compliance and data integrity. In this role you will mentor...DataWebsiteWorldwide
- ...Health seeks an Experienced Clinical Research Associate (CRA) with at least 1 year of independent monitoring experience for a homebased role... ...The candidate will perform site qualification, initiation,... ...ensuring GCP compliance and data integrity. Responsibilities include evaluating...DataWebsiteRemote work
- ...Parexel is seeking a Senior Clinical Research Associate (0.5 FTE) to join our team in Belgium in a remote/home-based capacity. You will oversee monitoring across investigator sites, ensuring data integrity, patient safety, and regulatory compliance in oncology trials within...DataWebsiteRemote workWork from home
$25.84 - $34.94 per hour
Research --> Support StaffNew York • ID... ...countless people. An integral part of NYU... ...team as a Research Associate.This role involves clinical research data collection, interaction... ...between study sites, clinical staff, and... ...and data management.Monitors study supplies and...DataWebsiteHourly payDaily paidFull timeCasual workRemote workDay shiftAfternoon shiftEarly shift- ...Worldwide Clinical Trials is seeking an experienced Clinical Research Associate to support site qualification, monitoring, and study close-out visits across trials. You will mentor... ...protocol adherence, safety reporting, and data integrity through on-site or remote reviews....DataWebsiteRemote workWorldwide
£6k per year
...ever wanted to see a clinical trial happen in... ...time? This is not monitoring from a distance. At... ..., CRAs are on site, in the flow of the... ...floor. You review data as it is generated... ...,000 ft² Clinical Research Unit, only 7 minutes... ...remote monitoring. Integrated eSource and EDC...DataWebsitePermanent employmentFull timeLive inCurrently hiringWork at officeRemote workFlexible hours- ...InnoCare has built up a fully integrated platform in terms of research and development, clinical development,... ...Responsibilties Conduct site selection, initiation, routine monitoring, and close-out visits per... ...plans. Perform source data review (SDR), source data...DataWebsiteWorldwide
$110k - $135k
...Companies is seeking a Senior Clinical Research Associate (CRA) to support a... ...clinical trial sites, ensuring compliance with... ...Conduct on-site and remote monitoring visits to ensure compliance... ...documentation, and data quality to maintain trial integrity and participant safety....DataWebsiteRemote work- ...world’s health. From clinical trials to regulatory,... ...biopharmaceutical companies and research sites to design and deliver... ...Clinical Research Associate (SCRA) to join our... ...trial quality, data integrity, patient safety, and... ...model, you will oversee monitoring activities across...DataWebsiteLocal areaRemote workWork from homeWorldwide
- ...sets us apart is the way we integrate clinical trial execution with deep... ...expertise and advanced data sciences. We have a... ...now recruiting Clinical Research Associate I/ Clinical Research Associate... ...position with travel to sites for monitoring visits. We are looking for...DataWebsiteLocal areaRemote workNight shift
- ...world’s health. From clinical trials to... ...year of independent monitoring) Key Accountabilities... ...contact with assigned sites, assess and ensure overall integrity of study implementation... ...evaluate potential data quality and data... ...experience in clinical research, with understanding...DataWebsiteLocal areaImmediate startRemote workFlexible hours
$50k - $70k
...member of the Alira Health Clinical team. In-house CRAs manage and support clinical sites from site approval through close... ...Managers to ensure the integrity of the trial data without the need for frequent... ...years of experience in clinical research TECHNICAL COMPETENCES & SOFT...DataWebsitePermanent employmentContract workLocal areaRemote work- ...II/Sr CRA I/II to work from home supporting ITA studies. You will perform site qualification, initiation, and monitoring visits across multiple sites to ensure GCP compliance and data integrity. Responsibilities include reviewing source documents, IP reconciliation, and...DataWebsiteRemote job
- ...world’s health. From clinical trials to... ...biopharmaceutical companies and research sites to design and... ...Research Associate (CRA) with Metabolic... .../MASH or Obesity monitoring experience to... ...accurate clinical data. You will conduct... ...execution. Oversee study integrity and build...DataWebsiteWork at officeWorldwideFlexible hours
- ...Clinical Research Associate – Full-Service Syneos Health is a fully integrated biopharmaceutical solutions organization... ...Responsibilities Perform site qualification, site initiation, interim monitoring, site management... ...affect subject safety and data integrity. Assess...DataWebsiteInterim roleLocal areaImmediate startRemote workFlexible hours
- Premier Research Group seeks a Clinical Research Associate II/Senior CRA - French Fluency to join our Clinical Monitoring, Site Management and SSU team in Quebec. You will monitor Phase... ...device studies, with a focus on data integrity and patient safety. You will travel...DataWebsiteRemote job
- Partner Company is seeking a Clinical Trial Monitor to oversee wound care studies with a focus on data integrity and regulatory compliance. You will conduct qualification and visitation activities across study sites, ensuring CRF accuracy and timely safety reporting. The...DataWebsiteRemote job
$80k - $105k
...CRA performs monitoring activities related... ..., quality data collection) and... ...and Hematology clinical trials within... ...milestones for sites responsible... ...the quality and integrity of site practices... ...of Clinical Research Coordinator... ...knowledge of ICH and associated regulatory...DataWebsiteHourly payContract workLocal areaWorldwide$51k - $82k
...in aviation, engineering, data science, and systems integration. At Peraton, you won’t... ...Peraton is seeking a IT Monitoring Administrator (... ...environment for a long-term, on-site engagement. The primary focus... ...2 years’ experience or Associate’s degree and 4 years’...DataWebsiteContract workShift workNight shiftAfternoon shift
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Associate: Site Monitor & Data Integrity. Be the first to apply!
- clinical research associate New York, NY
- regional clinical research associate New York, NY
- clinical trials assistant New York, NY
- clinical research assistant New York, NY
- clinical research administrator New York, NY
- senior clinical research associate New York, NY
- on-site clinical research associate (traveling/remote) New York, NY
- clinical research associate contract New York, NY
- clinical research associate cra New York, NY
- monitor technician New York, NY


