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Healthcare
› Clinical Research Associates
Clinical Research Associates
476 open positions
Sr CRA (Level I) - FSP
Thermofisher
Remote, Argentina
1mo
Senior Clinical Research Associate conducting risk-based monitoring, site management, and compliance assurance for oncology/hematology clinical trials.
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Clinical Research Associate (CRA) - Client-dedicated
Thermofisher
Remote, Turkey, TR
1mo
Conduct independent on-site clinical monitoring for pharmaceutical and clinical research organization clients to ensure study quality and regulatory compliance.
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Senior Clinical Research Associate
Msd
MYS - Selangor - Petaling Jaya (Ascent Paradigm), MY
1mo
Ensure performance and compliance of assigned clinical trial protocols and sites within the country, serving as the primary site contact and manager throughout all study phases.
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Clinical Research Associate (CRA) - Client dedicated (FSP)
Thermofisher
Remote, Egypt
1mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical and biotech clients.
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Lead Clinical Research Associate
Psi-Cro
Remote, US, us
1mo
Lead Clinical Research Associate providing leadership, oversight, and mentorship for regional clinical trials with minimal site assignments and a low-travel model.
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CRA I - FSP - Paris region
Thermofisher
Saint Aubin, France
1mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical and biotech sponsors.
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Clinical Research Associate II
Icon
Malaysia, Kuala Lumpur
1mo
Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials to ensure protocol compliance, data integrity, and patient safety.
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Clinical Research Associate
AbbVie
Seoul, Seoul, kr
1mo
Partner with investigative sites to ensure appropriate conduct of clinical trials, driving data integrity, compliance, and study performance for AbbVie's pipeline.
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Senior Clinical Research Associate
AbbVie
Seoul, Seoul, kr
1mo
Senior Clinical Research Associate leading site management, monitoring, and investigator engagement to ensure trial compliance, data integrity, and patient safety for AbbVie's clinical pipeline.
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Senior Clinical Research Associate I
Thermofisher
Remote
1mo
Performs and coordinates clinical monitoring and site management processes to ensure trial compliance with protocols, ICH-GCP guidelines, and regulations.
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CRA (Level II)
Thermofisher
Milan, Italy
1mo
Monitor clinical trial sites in Italy to ensure compliance with protocols, ICH-GCP guidelines, and regulations, focusing on patient safety and data integrity.
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Senior Clinical Research Associate I Sponsor-Dedicated FSP - Germany (m/f/d)
Thermofisher
Remote, Germany
1mo
Senior Clinical Research Associate conducting risk-based monitoring, site management, and compliance assurance for clinical trials across pharmaceutical and biotech sectors.
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FSP Sr CRA (Level I)
Thermofisher
Remote, Argentina
1mo
Senior Clinical Research Associate conducting risk-based on-site and remote monitoring to ensure protocol compliance, data accuracy, and subject safety across clinical trials.
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Clinical Research Associate - FSP - Czechia
Thermofisher
Remote, Czechia
1mo
Coordinate clinical monitoring and site management to ensure trials comply with protocols, ICH-GCP guidelines, and regulations, guaranteeing subject rights and data reliability.
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Clinical Research Associate (Biomedical Engineering Candidates)
Medpace
Irving (Dallas), Texas
1mo
Conduct qualification, initiation, monitoring, and closeout visits at research sites to ensure compliance with protocols and regulatory requirements for pharmaceutical and medical device development.
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FSP CRA (Level II)
Thermofisher
Remote, Colombia
1mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for clinical trials.
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FSP CRA (Level II)
Thermofisher
Remote, Mexico
1mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical and biotech clinical trials.
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Data Compliance Coordinator
Thermofisher
Birmingham, United Kingdom
1mo
Ensure data quality and regulatory compliance for clinical trials across research sites, coordinating operational activities and maintaining documentation.
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Senior Site Specialist
Icon
Remote
1mo
Operational point of contact for investigator sites in Poland, managing site start-up, maintenance, and close-out activities.
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Senior CRA
Psi-Cro
Skopje, SK, mk
2mo
Conduct and report onsite monitoring visits (SIV, RMV, COV), perform CRF review and source document verification, and manage clinical sites for Phase II/III studies.
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CRA Levels II/Sr - FSP - Portugal
Thermofisher
Remote, Portugal
2mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical and biotech clients.
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Senior Clinical Research Associate
Thermofisher
Brisbane, Australia
2mo
Monitor clinical trial investigator sites using risk-based approaches to ensure compliance with protocols and regulations, manage data accuracy, and resolve site deficiencies.
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FSP CRA(Level II)
Thermofisher
Chengdu, China
2mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical and biotech clinical trials.
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Clinical Research Associate II
Psi-Cro
Remote, US, us
2mo
Conduct on-site monitoring visits for clinical studies across various therapeutic indications, ensuring data integrity, compliance, and study supply management.
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Senior Clinical Research Associate
Psi-Cro
Remote, US, us
2mo
Conduct onsite monitoring visits, manage clinical sites and investigators, and ensure data compliance and subject safety across Phase I-III trials.
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Clinical Research Associate
Psi-Cro
Mexico City, CDMX, mx
2mo
Conducting clinical monitoring visits, training site staff, and managing complex clinical studies to ensure data quality and regulatory compliance.
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Senior Clinical Research Associate
Ergomed
Remote
2mo
Conducts on-site or remote monitoring visits (Pre-Study, Initiation, Interim, Close-Out) to ensure investigational sites and staff are adequate for clinical study conduct.
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Clinical Research Associate I (CRA I) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)
Thermofisher
Remote
2mo
Monitor clinical trial sites to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability and subject safety.
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CRA - FSP - Italy
Thermofisher
Milan, Italy
2mo
Clinical Research Associate monitoring investigator sites for pharmaceutical and biotech sponsors to ensure protocol compliance and data accuracy.
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Senior CRA - FSP - Medical Device - US Central/West Coast
Thermofisher
Remote, Montana, USA
2mo
Senior Clinical Research Associate conducting risk-based monitoring, site management, and audit readiness for medical device and pharmaceutical clinical trials.
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Sr CRA - FSP - Belgium & Netherlands
Thermofisher
Remote
2mo
Senior Clinical Research Associate conducting risk-based monitoring, site management, and regulatory compliance for pharmaceutical clinical trials.
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CRA (Paris, Lyon & Nantes)
Thermofisher
Ivry-sur-Seine, France
2mo
Clinical monitoring and site management for clinical trials, ensuring protocol and regulatory compliance across commercial and government contracts.
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Senior Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed
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Parexel
Uxbridge, England, UK
2mo
Manage assigned clinical trial investigator sites from activation through database lock, ensuring patient safety and quality study execution.
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Senior Clinical Research Associate/ Clinical Research Associate II
Psi-Cro
Ankara, Ankara, tr
2mo
Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications.
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Clinical Research Associate (CRA) - Dallas
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Medpace
Irving, TX
2mo
Conduct on-site and remote monitoring visits at clinical research sites to ensure protocol compliance, data accuracy, and patient safety during drug and medical device development.
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Senior Clinical Research Associate
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ICON Strategic Solutions
Washington, DC
$111k–$111k
2mo
Manage investigative sites for oncology clinical trials to ensure data integrity, subject safety, and inspection readiness.
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Clinical Research Associate - CRA (Level Depending on Experience)
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Cti Clinical Trial and Consulting Services
Sydney, New South Wales, Australia
2mo
Conduct on-site and remote monitoring of clinical trials for chronically and critically ill patient populations, ensuring data quality and regulatory compliance across the study lifecycle.
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Experienced Clinical Research Associate (Senior / CRA II)
Psi-Cro
Ra'anana, Center District, il
2mo
On-site monitoring of clinical studies across various therapeutic indications, ensuring data integrity, compliance, and site performance.
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Clinical Trial Site Relationship Coordinator (Hungarian Speaking)
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Medpace
London, England, UK
2mo
Manage strategic relationships with clinical trial sites in the UK and Hungary, conducting feasibility assessments and supporting study start-up.
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Entry Level - Clinical Research Associate
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Medpace
London, England, UK
2mo
Conduct on-site monitoring visits for clinical trials to ensure compliance with protocols, regulations, and data accuracy for drug and medical device development.
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Clinical Research Associate - Clinical Research Coordinator Experience
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Medpace
Cincinnati, OH
2mo
Conduct on-site and remote monitoring visits at clinical research sites to ensure protocol compliance, data accuracy, and patient safety for Phase I-IV clinical trials.
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Clinical Trial IWRS Monitor I
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Everest Clinical Research
Remote
$45k–$45k
2mo
Monitor data generated within Clinical Trial Technology (CTT) applications to ensure accuracy and quality, acting as the primary contact for users and supporting the IWRS/IRT and eDiary team.
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Clinical Trial IWRS Monitor (Overnight)
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Everest Clinical Research
Remote
$45k–$45k
2mo
Provide overnight monitoring and support for Clinical Trial IWRS/IRT systems, ensuring data accuracy, resolving client issues, and supporting system testing and documentation.
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Bilingual Clinical Research Associate (CRA) - Montreal
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Medpace
Remote
2mo
Conduct pre-study, initiation, monitoring, and closeout visits for clinical research sites to ensure compliance with SOPs and GCP.
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Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
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Medpace
Phoenix, AZ
2mo
Conduct qualification, initiation, monitoring, and closeout visits at research sites to ensure compliance with protocols and regulations.
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Experienced CRA Manager
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Medpace
Munich, Bavaria, Germany
2mo
Managing and developing Clinical Research Associates (CRAs) to ensure study monitoring consistency, compliance, and performance standards for clinical trials.
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CRA (Level I or II) FSP - Athens
Thermofisher
Remote, Greece
2mo
Conduct remote and on-site clinical monitoring visits to assess protocol and regulatory compliance, manage site processes, and ensure data reliability for pharmaceutical and biotech clinical trials.
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Clinical Research Associate / Senior Clinical Research Associate
Psi-Cro
Munich, BY, de
2mo
Conduct onsite and remote monitoring visits, perform CRF review and source document verification, and manage clinical sites for Phase II/III AMG studies.
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CRA II and SR CRA
Icon
Remote
2mo
Clinical trial monitoring and site relationship management for global healthcare clinical programmes.
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(Asso./Sr.) Manager, Country Clincial Quality Management
Msd
CHN - Beijing - Beijing (Wangjing Park), CN
2mo
Ensure patient safety, high-quality data, and regulatory compliance for company-sponsored clinical trials at the country level.
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