Clinical Research Associate - Monitor Trials & Data Integrity
ICON Strategic Solutions
ICON is a global healthcare intelligence and clinical research organization focused on speeding the delivery of new medicines and treatments. As a CRA at ICON, you will design and analyze clinical trials, interpreting complex medical data and contributing to innovative therapies. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety throughout the trial process. Travel about 60% is expected. #J-18808-Ljbffr ICON Strategic Solutions
- Dana-Farber Cancer Institute in Boston seeks a Clinical Trials Monitor to ensure regulatory compliance across the DF/HCC consortium. The role... ...as needed while upholding Dana-Farber's standards for ethics and data integrity. #J-18808-Ljbffr Dana-Farber Cancer InstituteDataRemote work
- Syneos Health is actively seeking a Clinical Research Associate to support full-service monitoring across sites in the United... ...site qualification, and timely data capture, with on-site or remote... ...maintaining high safety and data integrity standards. #J-18808-Ljbffr Syneos...DataRemote job
- Alira Health Group is seeking a Clinical Research Associate to join its Boston team. The CRA will conduct site monitoring for clinical trials and ensure compliance with regulations. Responsibilities include overseeing trial management, coordinating with cross-functional...SuggestedRemote job
- Merck & Co., Inc. seeks a Clinical Research Associate (site management) to ensure study conduct... ...site relationships across trials. The role requires oversight of monitoring activities, regulatory documentation... ...initiation, monitoring visits, data quality reviews, and effective...DataRemote job
- PSI CRO is seeking a Clinical Research Associate to monitor clinical studies in various therapeutic indications with a focus on data integrity and compliance. You will act as the main liaison between the project team, sponsor, and site, building strong site relationships...Data
- Getinge is looking for a Senior Clinical Research Associate based in Boston, MA. This role involves managing... ...solid organ platforms to ensure data quality and compliance with regulations... ...over 6 years of experience in clinical trials, preferably in medical devices or pharmaceuticals...Data
$67.5k - $99k
## Clinical Trial AdministratorApplylocations: Cambridge (US)time type... ...unmet medical need through research and innovation. Our... ...Technical Competencies****Set-up, monitoring, verifying and archiving the... ...the SP/Ipsen to maintain data integrity and to ensure eTMF inspection...DataContract workTemporary workWork experience placementLocal areaFlexible hours- Syneos Health in the United States is seeking a Clinical Research Associate - Full-Service to support remote site monitoring and trial coordination. The role covers site qualification, initiation visits, data verification, IP handling, and close-out activities, requiring...DataRemote job
$98.9k - $108.4k
The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, state,... ...will be performed through a combination of remote data review and onsite monitoring visits; therefore,...DataInterim roleWork at officeLocal areaRemote work- ...Biosciences is seeking a Global Monitoring Manager / Associate Director to lead... ...activities across global trials, ensuring adherence to protocol... ...oversee CRAs and CROs, drive data quality, patient safety,... ...requires 7-10 years in clinical research, leadership experience, and...DataRemote work
- myBridge Corporation is seeking a dedicated clinical research professional to monitor trials and ensure regulatory compliance. The role involves coordinating... ...proficient in GCP, FDA regulations, documentation, and data analysis. Strong communication skills are essential to...Data
- ...intelligence and clinical research organisation united... ...organisation, integrity, collaboration, agility... ...manage clinical trial activities to... ...You Will Be Doing:Monitoring clinical trial... ...timely and accurate data collection and... ...Clinical Research Associate, with a strong understanding...DataFull time
- ...are seeking Experienced Clinical Research Associates to join our team. We are... ...in hematology/oncology monitoring, which includes a general... ...against case report form data, including informing the... ...review) through our integrated Clinical Trial Management System to identify...DataContract workWork at officeRemote workWork from home
- ...has built up a fully integrated platform in terms of research and development, clinical development, manufacturing... ..., initiation, routine monitoring, and close-out visits... ...plans. Perform source data review (SDR), source... ...years of direct oncology trial monitoring experience...DataWorldwide
- ...Mass General Brigham Clinical Research Regulatory CoordinatorMass General... ...requirements for clinical trials are met. This position involves... ...entities.Participate in monitoring visits and maintain a... ...to recognize compliance and data integrity issues and respond appropriately...DataContract workRemote work
- ...the Alira Health Clinical team. The CRA is... ...to conduct site monitoring responsibilities for clinical trials; as well as providing... ..., in‑house CRAs, Associate Director of... ...status. Ensures integrity of CRF data through meticulous... ...Knowledge of clinical research, ICH GCP and...DataContract workInterim roleLocal areaRemote work
- ...Description Experienced Clinical Research Associate - Sponsor Dedicated... ...is a leading fully integrated biopharmaceutical... ...initiation, interim monitoring, site management activities... ...safety and clinical data integrity at an... ...of the ISF with the Trial Master File (TMF)....DataContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- AbbVie seeks a Clinical Research Associate to advance our clinical programs, partnering with investigators and site staff to ensure compliant execution and high-quality data. You will monitor site activities, train personnel, and drive patient recruitment while maintaining...Data
$30 - $40 per hour
...Shaping the Future of Clinical ResearchAdams... ...leading clinical trial site network committed... ...uncompromising data quality, safety, and... ...in clinical research and want to be part... ...Psychedelic Dosing Monitor to support clinical... ...standards to support data integrity and participant...DataHourly payDaily paidReliefFlexible hours3 days per week$50k - $70k
...important member of the Alira Health Clinical team. In-house CRAs manage and support... ...Project Managers to ensure the integrity of the trial data without the need for frequent travel.... ...~1-2 years of experience in clinical research Technical Competences & Soft Skills...DataPermanent employmentContract workLocal areaRemote work- ...is seeking an In-house CRA to join our Clinical team. The role manages and supports clinical... ...Project Managers. You will ensure data integrity, help prepare ICFs and regulatory submissions... ...with site performance and training to support trials. #J-18808-Ljbffr Alira HealthDataRemote job
- Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on... ...information flow with trial sites on Adverse Events... ...deviations Perform source data verification and... ...quality (data integrity and compliance) at site...DataWork visa
- ...striving for excellence in clinical research, turning science into medicine... ...as the choice in clinical trials. Focus on site clinical... ...while driving improvement in data integrity, compliance, overall study... ...routine, and site closure monitoring activities with compliance...DataFull timeContract workTemporary workLocal area
- ...are seeking Experienced Clinical Research Associates to join our team. We are... ...in hematology/oncology monitoring, which includes a general... ...against case report form data, including informing the... ...review) through our integrated Clinical Trial Management System to identify...DataContract workWork at officeRemote workWork from homeHome officeFlexible hours
- ...Senior Clinical Research Associate (Level I) As part of the Thermo... ...What You'll Do: Monitors investigator sites with... ...decrease risks. Ensures data accuracy through SDR,... ...Provides trial status tracking and progress... ...common set of values - Integrity, Intensity,...DataWork at officeRemote workHome officeFlexible hours
$65 - $76 per hour
...Lead Dosing Session Monitor Boston, Massachusetts... ...Shaping the Future of Clinical Research Adams Clinical is a leading clinical trial site network committed... ...deliver uncompromising data quality, safety, and... ...through innovation and integrity If you're passionate...DataHourly payPart timeRemote work3 days per week- ...Senior Clinical Research Associate (Level II) As part of the Thermo... ...What You'll Do: Monitors investigator sites with... ...decrease risks. Ensures data accuracy through SDR,... ...Initiates clinical trial sites according to... ...common set of values - Integrity, Intensity,...DataWork at officeRemote workRelocationHome officeRelocation packageFlexible hoursNight shift
- ...business people, tech experts, researchers, and systems analysts to... ...is seeking a highly motivated Clinical Research Assistant II to join... ...translational research and clinical trial program.This individual will... ...and organizing patient data; scheduling patients for study...DataRemote work
- ...Biosciences is seeking a Global Monitoring Manager / Associate Director to lead... ...activities across global trials, ensuring compliance with... ..., drive site performance, data quality, and inspection readiness... ...requires 7-10 years in clinical research with lead experience, willingness...DataRemote job
- ...people, tech experts, researchers, and systems... ...Summary Conduct site monitoring visits in... ...to CRFs to ensure data is complete and accurate... ...the course of the trial Review study-specific... ...1-2 years of clinical research experience... ...leadership role as an integrated health care system...DataFull timeWork at officeRemote workMonday to FridayShift work
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