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Healthcare
› Clinical Research Associates
Clinical Research Associates
553 open positions
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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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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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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Senior CRA level I
Thermo Fisher Scientific
México
2mo
Conduct remote or on-site clinical monitoring and site management to ensure protocol and regulatory compliance, manage documentation, and guarantee subject rights and data reliability for pharmaceutical and biotech clinical trials.
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Sr. CRA 3, Brazil, IQVIA Biotech
Iqvia
Brasil
2mo
Independently manage and monitor clinical trial sites to ensure compliance with protocols, GCP, and ICH guidelines, supporting patient recruitment and data quality.
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Clinical Line Manager - CRA (Based in Navi Mumbai, India)
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Medpace
Navi Mumbai, Maharashtra, India
2mo
Lead and line-manage a team of Clinical Research Associates (CRAs) to ensure they meet core monitoring responsibilities and company objectives.
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Clinical Research Associate
Ire
São Paulo, Estado de São Paulo
2mo
Conduct clinical trial monitoring to ensure study compliance, patient safety, and data accuracy across clinical programmes.
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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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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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Clinical Trial Site Relationship Coordinator (Finnish 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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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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Senior Clinical Research Associate (Oncology Experience Required) - UK (Remote) - FSP - REGISTER YOUR INTEREST
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Parexel
Remote
2mo
Senior Clinical Research Associate ensuring data integrity, compliance with ICH GCP, and protocol adherence at clinical trial sites, with a focus on oncology trials.
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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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Bilingual Clinical Research Associate (CRA) - Montreal
↗
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 Trial IWRS Monitor (Overnight)
↗
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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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 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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Senior Clinical Research Associate I (SCRA I)
Pfizer
Argentina - Remote
2mo
Oversee site management, monitoring, and close-out operations for clinical trials, ensuring compliance and patient safety while mentoring junior CRAs.
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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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Clinical Research Associate II
Corcept Therapeutics
Redwood City, California, United States
$129k–$129k
2mo
Monitors clinical study activities to assure adherence to Good Clinical Practices (GCPs), Standard Operating Procedures (SOPs), and study protocols.
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Central Review Manager (Senior)
Thermofisher
Mexico City, Mexico
2mo
Perform centralized review and approval of clinical monitoring visit reports (PSA, SI, ME, CO) to ensure protocol adherence, subject safety, and study process compliance.
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CRA II
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Fortrea
Maidenhead, England, UK
2mo
Lead and manage clinical trial sites across diverse and complex therapeutic areas including oncology, neuroscience, and cell & gene therapy.
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Clinical Research Associate II - Sydney
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Fortrea
Sydney, New South Wales, Australia
2mo
Managing and monitoring clinical trials to ensure compliance with regulatory requirements and data integrity while fostering relationships with investigative sites.
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Centralized Clinical Trial Manager
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ICON Plc
Bengaluru, Karnataka, India
2mo
Reviewing clinical trial site visit reports to ensure quality, minimize errors, and escalate issues; acting as a liaison between monitoring and management teams.
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CRA
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ICON Plc
Reading, England, UK
2mo
Required skills: Advanced degree in a relevant field such as life sciences, nursing, or medicine, Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements, Proven ability to…
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FSP Sr CRA (Level I)
ThermoFisher Scientific
México
2mo
Senior Clinical Research Associate conducting risk-based monitoring, site initiation, and close-out for oncology clinical trials.
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CRA
Icon
UK, Reading
2mo
Overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards while ensuring data integrity and participant safety.
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Sr CRA I/II - FSP - Norway
Thermofisher
Remote, Norway
2mo
Senior Clinical Research Associate conducting risk-based monitoring, site management, and regulatory compliance for clinical trials in oncology and cell therapy.
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Clinical Research Associate 2 - Multi-Sponsor - Based in Madrid or Barcelona
Iqvia
España
2mo
Conducting site selection, initiation, monitoring, and close-out visits for clinical trials while ensuring data integrity and regulatory compliance.
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CRA / Sr CRA
ThermoFisher Scientific
México
2mo
Monitor and manage clinical trial sites to ensure compliance with protocols, regulations, and patient safety standards.
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Senior CRA I
ThermoFisher Scientific
México
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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CRA II, London (client-dedicated)
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Fortrea
Maidenhead, England, UK
2mo
Conduct and oversee study site monitoring visits to ensure compliance with protocols and regulatory requirements, managing site initiation, monitoring visits, and closeouts.
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Entry-level Clinical Research Associate - Clinical Research Coordinator experience
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Medpace
2mo
Conduct on-site and remote monitoring visits at clinical research sites to ensure protocol compliance, data accuracy, and regulatory adherence for pharmaceutical and medical device trials.
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Clinical Research Associate Entry (Melbourne)
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Medpace
South Yarra, Victoria, Australia
2mo
Conducting qualification, initiation, monitoring, and closeout visits for research sites to ensure compliance with protocols and regulatory requirements.
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Clinical Research Associate (Home-based, Sydney)
↗
Medpace
Sydney, New South Wales, Australia
2mo
Conduct on-site monitoring visits for clinical research sites to ensure compliance with protocols, verify data accuracy, and manage investigational product accountability.
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CRA I/II - FSP
Thermofisher
Remote, Germany
3mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance for oncology and cell therapy trials.
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Clinical Operations Lead (Tokyo or Osaka)
Psi-Cro
Tokyo, Tokyo, jp
3mo
Lead line management and mentoring of Clinical Research Associates (Monitors) for site selection, initiation, monitoring, and closeout visits in clinical trials.
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CRA / Sr CRA
Thermofisher
Remote, Argentina
3mo
Monitor and manage clinical trial sites to ensure compliance with protocols, ICH-GCP guidelines, and regulatory requirements while safeguarding patient safety and data integrity.
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Assistant CRA
Thermofisher
Remote, United Kingdom
3mo
Supports Clinical Research Associates with remote monitoring, site preparedness, logistics, and document management to ensure high-quality clinical trial execution.
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