Remote Clinical Research Associate: Trials & Compliance
Thornton Tomasetti
- Remote job
Abbott is seeking a Clinical Research Associate to support site monitoring from start-up through closeout, ensuring compliance with protocols and regulatory requirements. The role partners with Clinical Project Teams and Operations, working in a regulated quality environment to meet study timelines. Based remotely in the United States near a major airport or at an Abbott office, travel is up to 40%. The position requires at least 1 year of clinical research experience and strong communication #J-18808-Ljbffr Thornton Tomasetti
- 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... ...timely safety reporting. The role offers remote work options within the United States,...Remote job
- ...Establishment Labs is seeking a Senior Clinical Research Associate to manage and monitor clinical... ...start-up through closeout, ensuring compliance with GCP, ICH, FDA and global requirements... ...quality and regulatory activities in a remote setting. You will coordinate sites...Remote work
$95k - $125k
OverviewThe Clinical Research Associate (CRA) supports clinical trial quality, compliance, and execution through site monitoring, study startup, data oversight, and regulatory... ...-out visits as required.Perform SDV, SDR, remote monitoring, data review, query management, and...Remote workWork at officeLocal area- AmsterdamClinical Services - Clinical Study Delivery - Monitoring &... ...assessing protocol and regulatory compliance as per Alimentiv’s and... ...conduct and document onsite and remote activities, including site... ...Experience with Phase I-IV clinical trials is preferred.• Thorough...Remote workFull timeWork at officeLocal area
- Regional Clinical Research Associate IIBIOTRONIK is one of the leading manufacturers of... ...team. Conduct on-site, remote, and centralized monitoring to ensure compliance with FDA regulations, ICH/GCP... ...supporting medical device IDE trials is preferred.Strong clinical...Remote workFull timeContract workWork at officeHome office
- ...cervical spine conditions is seeking a Clinical Research Associate. Responsibilities include managing clinical trials, ensuring compliance, and coordinating operations with study... ...medical device field. This role allows for remote work and offers opportunities to...Remote work
- ...Consultant, Clinical Site Lead, Medical Devices Summary Our... ...and field monitoring to ensure compliance with protocols, regulations,... ...field. ~3-5+ years of clinical trial monitoring experience... ...environment. Term & Start ~ Remote/home-based; Ideally located...Remote workContract workPart timeLocal areaWork from home
- ...To support a global clinical program, the fully remote Oncology Clinical Research Associate will conduct site visits, ensure compliance with regulatory standards, and collaborate with investigative... ...adherence, and maintain essential trial documentation to support regulatory...Remote workWork at office
- ...To support clinical trial initiatives, the freelance Clinical Research Associate (0.4 FTE) will conduct remote and on-site monitoring, ensuring compliance with regulatory requirements and data integrity while working fully remotely. Key Responsibilities: Monitor clinical...Remote workFreelance
$50k - $70k
...member of the Alira Health Clinical team. In-house CRAs... ...the integrity of the trial data without the need... ...to ensure protocol/GCP compliance, assesses subject... ...requests Conducts remote review of data entered... ...experience in clinical research TECHNICAL COMPETENCES...Remote workPermanent employmentContract workLocal area- ...Clinical Research Associate (CRA) At Thermo Fisher Scientific, you'll discover... ...changing therapies. With clinical trials conducted in 100+ countries... ...process. Conducts remote or on-site visits to assess protocol and regulatory compliance and manages required documentation...Remote workWork at officeLocal areaFlexible hours
$120k - $135k
...Company & Job Overview: The Clinical Research Associate (CRA) will support Clinical Operations... ..., and executing Diality clinical trials in compliance with applicable regulations (e.g.,... ...Clinical Monitoring: Perform remote monitoring activities such as source...Remote workFull timeContract workWork at office- ## Experienced Clinical Research Associate - Sponsor DedicatedApply: Remote (Pre-Approved): USA-NC-Remote: USA-RI-Remote: USA... ...Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experience to... ...contents of the ISF with the Trial Master File (TMF). Ensures the...Remote workFull timeContract workInterim roleLocal areaImmediate startFlexible hours
- ...Clinical Research Associate (Level II) Join Us as a Clinical Research Associate... ...biotechs, spanning 2,700 clinical trials across 100+ countries in... ...(Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required...Remote workWork at officeHome officeFlexible hoursNight shift
- ...Sr. Clinical Research Associate The Senior Clinical Research Associate will play... ...group, ensuring full compliance with regulatory requirements... ...clinical research in drug trials, including Good Clinical Practice... ...performing on-site and/or remote site qualification visits,...Remote workInterim roleWork at officeLocal areaFlexible hoursShift work
- ...Cedars-Sinai! The Angeles Clinic & Research Institute has... ...Clinical Research Data Associate II manages the data for... ...to develop and maintain trial management systems. Ensures compliance with all federal and local... ...onsite and 1 day per week remote. Please note that fully...Remote workLocal area1 day per week
- ...accelerating innovation from concept to patient impact. The Clinical Research Associate II role involves coordinating site initiation, monitoring, and close-out visits across medical device trials, ensuring GCP compliance and regulator readiness. You will train sites on the...
- ...Medical Center in Los Angeles seeks a Clinical Research Associate I to support study coordination, data collection, and regulatory compliance. You will work with a Clinical Research... ...Coordinator or Research Nurse to implement trials, collect CRFs, and ensure adherence to...
- Montefiore Hudson Valley Collaborative seeks a Research Associate I to manage multiple clinical trials as a patient-facing liaison and trial team lead. You... ...activities, maintaining protocol integrity and regulatory compliance. The role requires a Bachelor’s degree, GCP...
- ...Clinical Research Associate/Clinical Trial Monitor The Clinical Research Associate/Clinical Trial Monitor will... ...the conduct of the trial is in compliance with protocols, current Good Clinical... ...monitoring activities to include remote review of electronic source...Remote workContract workWork at office
- CTI Clinical Trial and Consulting Services is seeking a Clinical Trial Monitor to act as the primary CTI contact for assigned study sites... ...will conduct PSV, SIV, IMV, and COV visits, ensure regulatory compliance, and support start-up activities, site selection, and data/...
$129.4k - $152.3k
...Therapeutics in Redwood City, California is hiring a Clinical Research Associate II to monitor clinical study activities and ensure compliance with Good Clinical Practices and study... ...study preparation, coordinate clinical trial components, and liaise with vendors and...$97k - $193k
...Senior Clinical Research Associate role supporting CNS and rare disease studies across... ...closeout, including regulatory compliance, data quality, and safety reporting. Remote position with required regional... ...compliance at assigned clinical trial sites Conduct site...Remote workContract workWork at office$97k - $193k
...Senior Clinical Research Associate position focused on oncology site management for a... ...study initiation, regulatory compliance, and site closeout activities, primarily remote with regional travel required... ...research activities at clinical trial sites including site...Remote workWork at office- ...ProPharma Group seeks a Senior Clinical Research Associate with Alzheimer's disease... ...monitoring activities for clinical trials, manage site operations, and ensure regulatory compliance across assigned studies.... ...visits, both in-person and remote, including initiation and...Remote workWork at officeLocal area
$97k - $193k
...Senior Clinical Research Associate position overseeing site management and regulatory compliance for rare disease and oncology clinical trials. Remote role based on East Coast or Central US, requiring extensive experience managing research activities across trial phases...Remote workWork at office- ...Biotechnology Inc. is seeking a Senior Clinical Research Associate for a remote position based near Los Angeles, CA. The... ...Puma and investigative sites to ensure trials are conducted on time, within budget, and in full compliance with ICH GCP. The role covers in-house and...Remote job
- CND is seeking a Clinical Research Associate to oversee and monitor clinical trials at the Scottsdale site and collaborate with investigators and partners. The CRA ensures adherence to trial protocols, GCP guidelines, and timelines while maintaining high professional standards...3 days per week
- Worldwide Clinical Trials is seeking an experienced Clinical Research Associate to support site qualification, monitoring, and study close-out visits across trials. You... ..., and data integrity through on-site or remote reviews. The role requires 5+ years in CRA, a 4-...Remote workWorldwide
- A leading medical technology company is seeking a Remote Regional Clinical Research Associate II. This role involves conducting monitoring visits and ensuring compliance with regulatory standards. Ideal candidates have a Bachelor's degree in nursing or a life science, 3...Remote workWork from home
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Remote Clinical Research Associate: Trials & Compliance. Be the first to apply!
- clinical research associate Sacramento, CA
- clinical trials assistant Sacramento, CA
- clinical research assistant Sacramento, CA
- clinical research administrator Sacramento, CA
- on-site clinical research associate (traveling/remote) Sacramento, CA
- remote recruitment consultant Sacramento, CA
- remote data manager Sacramento, CA
- benefits specialist remote Sacramento, CA
- remote video game Sacramento, CA
- remote typing work Sacramento, CA



