Clinical Research Associate: Site Monitoring & Trials Support
$53 - $69 per hourOxford Global Resources
Oxford Global Resources is seeking a professional to support the Clinical Affairs team in ensuring compliance with clinical studies. The ideal candidate will have 2+ years of experience in a clinical research setting, proficiency in Microsoft Office, and will assist in various responsibilities including site monitoring and maintenance of trial master files. This role requires excellent communication skills and the ability to travel up to 50%. Competitive hourly rates of $53-69 are offered. #J-18808-Ljbffr
- A leading clinical research organization based in Boston seeks a Clinical Research support specialist. The role involves assisting in protocol... ...clinical documents, monitoring ongoing studies, and reporting... ...contribute significantly to clinical trials and their compliance. #J-188...Website
- Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Boston, Massachusetts. The Sr. CRA will be responsible for site management, monitoring, and close-out of clinical trials, ensuring patient safety and quality. Applicants should have a Bachelor's degree...Website
- ...Parexel is seeking a Senior Clinical Research Associate (Sr. CRA) in Boston, MA. The Sr. CRA will manage and monitor clinical trial sites to ensure patient safety, compliance with regulations... ...collaboration with the study team to support recruitment and monitoring activities....Website
- Beth Israel Lahey Health is seeking a Clinical Trials Monitor (CTM) based in Boston, Massachusetts.... ...The CTM will oversee and audit clinical research studies across various disease groups,... ...position may require occasional on-site work and involves detailed reviews of...WebsiteRemote jobCasual work
$58.24k - $90k
...difference in people’s lives. The Clinical Trials Monitor (CTM) monitors and audits... ...-initiated clinical research studies across all disease... ...remote but may require some on site work. Job Description:... ...SOPs, study protocols and supporting documents. (essential) Reviews...WebsiteFull timeWork experience placementWork at officeRemote work$101.6k - $169.3k
...A global clinical research organization is seeking a Senior Clinical Research Associate in Boston to oversee oncology study monitoring and site management. This role demands at least 2 years of on-site monitoring experience, along with a Bachelor's degree in a scientific...Website$67.5k - $99k
...Cookie NoticeClinical Trial Administrator page is loaded## Clinical Trial... ...and Neuroscience. Supported by nearly 100 years... ...medical need through research and innovation. Our... ...responsible for setting-up, monitoring, verifying and... ...the country and site binders and the trial...WebsiteContract workTemporary workWork experience placementLocal area$60 - $70 per hour
...Pharmaceuticals in Boston, Massachusetts, is seeking an EM/UM Technical Support, Quality Control Microbiology professional. This position... ...offers a pay range of $60-$70 per hour and is a 12-month on-site contract with potential for extension. #J-18808-Ljbffr Vertex PharmaceuticalsWebsiteHourly payContract work- ...Are you passionate about clinical research and ready to make an impact on patients... ...for a Clinical Research Associate (CRA) to join a fast-growing... ...What You'll Do: Conduct site initiation, monitoring, and close-out visits to ensure trials meet the highest quality standards...Website
- ...Title Responsible for providing Clinical Research support for all clinical trials. Under the direction of... ...evaluation of potential clinical sites according to established criteria... ...materials. Conduct ongoing study monitoring, including frequent periodic site...Website
- ...Job Purpose: The Clinical Research Associate (CRA) has local responsibility... ...at allocated sites and is an active... ...responsibility for monitoring the study conduct to... ...the study. Trains, supports, and advises Investigators... ...quality clinical trials with reduced budget...WebsiteLocal areaRemote workFlexible hoursShift work
- ...Description Join Us as a Clinical Research Associate (Level II) – Make an... ...have successfully supported the top 50... ...spanning 2,700 clinical trials across 100+ countries... ...1 year of travel monitoring experience in Neurology... ...monitoring and site management process....WebsiteWork at officeRemote workHome officeNight shift
- Clinical Research Associate, Sponsor Dedicated ICON plc is a world-... ...and analyze clinical trials, interpreting complex... ...contribute to clinical trial monitoring activities, taking... ...: Conducting site qualification, initiation... ...who are there to support you and your family’s...WebsiteFlexible hours
- ...A leading clinical research organization based in Boston is seeking a Clinical Research Associate (CRA) to support clinical trial operations across AFT studies. The ideal candidate will manage site operations and facilitate compliance with ICH GCP guidelines. Responsibilities...Website
- ...Clinical Research Associate The Alliance for Clinical Trials in Oncology Foundation (Foundation) is a foundation... ...of the Foundation in support of the Alliance,... ...is responsible for key site management and study... ...and rosters; reviewing monitoring reports to identify deficiencies...WebsiteRemote work
$79k - $100k
Public Health Consultant - Monitoring, Evaluation & Quality Improvement Type Full time Description... ...community health assessment (CHA/CHIP) support, epidemiologic assessments, and QI... ...work, with occasional travel to client sites, conferences, or meetings as required....WebsiteFull timeTemporary workLocal areaRemote workVisa sponsorshipWork visa$110k - $135k
...currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Boston... ...in ongoing Clinical Trials throughout the Country for a leading... ...Organization. Responsibilities Conduct site and study visits and perform all site monitoring activities across multiple...WebsiteRemote work$101.6k - $169.3k
...Senior Clinical Research Associate 1 Experience in oncology, cardiovascular, renal... .... Job Overview Perform monitoring and site management work to ensure... ...generation and resolution. May support start‑up phase. Ensure... ...available for filing in the Trial Master File (TMF) and...WebsiteFull timePart timeLocal areaImmediate start- ...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... ...or F2F). Provide enrollment support and ensure progress by...WebsiteLocal areaRemote work
- ...Alira Health Boston, LLC is seeking a Clinical Research Associate who will play a vital role in the monitoring of clinical trials. Responsibilities include conducting site evaluations, ensuring adherence to protocols, and collaborating with clinical teams to enhance project...Website
- ...Summary The Senior Clinical Research Associate (SrCRA) has local responsibility... ...at allocated sites and is an active... ...responsibility for monitoring the study conduct to... ...the study. Trains, supports, and advises Investigators... ...quality clinical trials with reduced budget...WebsiteLocal areaRemote workFlexible hoursShift work
- CTTX Health is seeking a Clinical Research Associate (CRA) to support innovative therapies in neuroscience. The ideal candidate will conduct trial site initiation, monitoring, and close-out visits, ensuring the highest quality standards are met. Candidates should have a...Website
$110k - $135k
...currently seeking an Oncology Clinical Research Associate (CRA) for an opportunity in Boston... ...in ongoing Clinical Trials throughout the Country for a leading... ...Organization. Responsibilities Conduct site and study visits and perform all site monitoring activities across multiple...WebsiteRemote work- ...Clinical Research Associate (CRA) Do you have expertise in complex clinical trial monitoring (like oncology)? Are you ready to make a difference in... ...medicines. In Cell Therapy Site Management & Monitoring (... ...investigators and support site feasibility. Manage...WebsiteFull timeContract workWork at officeLocal areaRemote workFlexible hours
- ...Clinical Research Associate, Home-based in Australia ICON is a global... ...and analyzing clinical trials, interpreting complex medical... ...be doing Conducting site qualification, initiation, monitoring, and close-out visits... ...package designed to support your health, wellbeing,...WebsiteWork from home
$85k - $125k
...member of the Alira Health Clinical team. The CRA is highly... ...to conduct site monitoring responsibilities for clinical trials; as well as providing oversight... ...copies for TMF filing. Supports audit readiness by submitting... ...necessary. Supports research sites with local...WebsiteContract workWork at officeLocal areaRemote workFlexible hours- ...Clinical Research Associate (CRA) When our values align, there's no... ...health. From clinical trials to regulatory, consulting... ...year of independent monitoring). Key... ...contact with assigned sites, assess and ensure overall... ...staff. Facilitate and support site with access to relevant...WebsiteLocal areaImmediate startRemote workFlexible hours
- ...role is responsible for supporting monitoring and site management activities for... ...collaboration with cross-functional clinical study teams and... .... Partner with Clinical Trial Liaison (CTL) and other client... ..., assess CRO Clinical Research Associate (CRA) and Investigator...WebsiteInterim roleWork at officeLocal areaRemote work
- ...Conduct site monitoring visits in accordance with standards of practice... ...through the course of the trial. Review study‑specific site... ...communication with assigned sites to support site enrollment, data entry... ...At least 1-2 years of clinical research experience required....WebsiteWork at office
$131k - $150k
Sr. Clinical Research Associate About Servier Servier in the U.S. is a... ...effective management and monitoring of clinical studies in the site(s) assigned by the... ...study related manuals and supportive documents if needed... ...progress of clinical trials and ensure the quality...WebsiteContract workTemporary workLocal areaRemote workFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Associate: Site Monitoring & Trials Support. Be the first to apply!
- on-site clinical research associate (traveling/remote) Dedham, MA
- junior website developer Dedham, MA
- clinical trial associate Dedham, MA
- clinical research nurse Dedham, MA
- clinical research physician Dedham, MA
- community support Dedham, MA
- app support Dedham, MA
- part time support Dedham, MA
- medical support Dedham, MA
- support services Dedham, MA

