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Healthcare
› Clinical Research Associates
Clinical Research Associates
476 open positions
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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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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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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Clinical Research Associate 2 or Senior Clinical Research Associate 1 (m/w/d), Single Sponsor
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Iqvia
Remote
2mo
Conducting site selection, initiation, monitoring, and close-out visits for clinical trials while ensuring data integrity and regulatory compliance.
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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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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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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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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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CRA I/II - FSP
Thermofisher
Remote, Germany
2mo
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
2mo
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
2mo
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
2mo
Supports Clinical Research Associates with remote monitoring, site preparedness, logistics, and document management to ensure high-quality clinical trial execution.
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Assistant CRA
Thermo Fisher Scientific
España
3mo
Support Clinical Research Associates with site preparedness, logistical monitoring, and administrative tasks for clinical trials in the pharmaceutical/biotech industry.
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Assistant CRA
ThermoFisher Scientific
España
3mo
Support Clinical Research Associates with site preparedness, logistical monitoring, and administrative tasks for clinical trials.
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CRA II - Saudi Arabia
Thermofisher
Riyadh, Saudi Arabia
3mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical clinical trials.
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Senior CRA
Psi-Cro
Toronto, ON, ca
3mo
Conduct and report onsite monitoring visits (SIV, RMV, COV), perform CRF review, source document verification, and query resolution for clinical trials.
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CRA Manager
Msd
MYS - Selangor - Petaling Jaya (Ascent Paradigm)
3mo
Manage a team of 6-14 Clinical Research Associates (CRAs) to ensure strong monitoring, study performance, and site adherence to regulations and SOPs in clinical trials.
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Sr. Clinical Research Associate (Poland)
Alimentiv
Warsaw
3mo
Independently performs, coordinates, and oversees all aspects of clinical site monitoring services, assessing protocol and regulatory compliance for clinical studies.
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Clinical Research Associate / Senior - FSP - Remote
Parexel
Remote
3mo
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through database lock, ensuring relevant timelines and quality deliverables are met.
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Clinical Research Associate (various Levels)
Thermo Fisher Scientific
España
3mo
Conducting on-site monitoring visits to ensure clinical trial data integrity and regulatory compliance for pharmaceutical studies.
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CRA - FSP - Central/Southern Poland
Thermofisher
Warsaw, Poland
3mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for pharmaceutical clinical trials.
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Clinical Research Associate (various Levels)
ThermoFisher Scientific
España
3mo
Support site preparedness, logistical monitoring, and administrative tasks for clinical trials in pharmaceutical and biotech sectors.
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Experienced CRA (multi-sponsor, multi-therapeutic, home-based and office-based positions available)
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Medpace
3mo
Conducting clinical monitoring visits at research sites to ensure protocol compliance, data accuracy, and patient safety across various therapeutic areas.
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Clinical Trial Site Relationship Coordinator
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Medpace
Munich, Bavaria, Germany
3mo
Manage strategic relationships with clinical trial sites, conduct feasibility assessments, and support study start-up across the DACH region.
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Clinical Research Associate I
Thermofisher
Remote, Costa Rica
3mo
Coordinate clinical monitoring and site management to ensure trial compliance with protocols, ICH-GCP guidelines, and regulations while guaranteeing subject rights and data reliability.
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CRA I - Senior CRA (FSP)
Thermofisher
Remote
3mo
Conducts remote and on-site clinical monitoring of investigator sites to ensure protocol and regulatory compliance, manage site processes, and guarantee data reliability for clinical trials.
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Clinical Research Associate, sponsor-dedicated Home Office - Deutschland
Fortrea
Remote
$0k–$0k
3mo
Managing all aspects of clinical study site selection and close-out for Phase I-III oncology trials in Germany.
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Clinical Operations Lead (Clinical Trial Manager)
Alimentiv
Frankfurt
3mo
Oversees clinical operations for a project at a regional or global level, managing deliverables, CRAs, and Investigator sites.
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CRA II, Oncology
Iqvia
Manchester, Greater Manchester
3mo
Conduct independent on-site monitoring visits for clinical trials to ensure protocol adherence and data integrity across diverse investigative sites.
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FSP Senior CRA
Thermofisher
Remote
3mo
Conduct remote and on-site clinical monitoring for complex oncology and cell/gene therapy studies to ensure protocol compliance, data accuracy, and site management.
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Senior Clinical Research Associate - Oncology, CNS, Rare Disease - UK
Worldwide Clinical Trials
UK
4mo
Ensuring clinical research programs are executed with quality and excellence by managing site visits, monitoring protocol adherence, and verifying data for oncology, CNS, and rare disease trials.
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Sr/CRA I/II - UK (numerous locations)
Thermofisher
Remote, United Kingdom
4mo
Clinical Research Associate performing end-to-end support for clinical trials from study start-up to close-out, ensuring protocol compliance and data reliability across UK sites.
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Clinical Research Associate 2 - Multi-Sponsor - Based in Madrid
Iqvia
Madrid
4mo
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 - Client decicated (FSP)
Thermofisher
Riyadh, Saudi Arabia
4mo
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 (Oncology Experience Required) - UK (Remote) - FSP - REGISTER YOUR INTEREST
Parexel
Remote
4mo
Senior Clinical Research Associate ensuring data integrity, compliance with ICH GCP, and protocol adherence at clinical trial sites.
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Principal CRA – Lead Monitor (m/w/d)
Thermofisher
Remote
4mo
Lead clinical monitoring and site management for complex, high-risk global clinical trials, ensuring compliance with ICH-GCP and EU regulations while mentoring junior staff.
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Part-Time CRA II - Klinischer Monitor (0.8 FTE) (m/w/d)
Thermofisher
Remote
4mo
Conducts clinical monitoring and site management for global clinical trials, ensuring protocol and regulatory compliance while managing investigator sites and data accuracy.
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Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane
Thermofisher
Brisbane, Australia
4mo
Perform clinical monitoring and site management for sponsor-driven trials, ensuring protocol and regulatory compliance.
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Sr. CRA (Level 1)
Thermofisher
Remote, Brazil
4mo
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, Site Management - Italy
Iqvia
Milano, Provincia di Milano
4mo
Perform monitoring and site management to ensure clinical study sites conduct trials per protocol and regulations.
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CRA II / Sr CRA - FSP - Austria
Thermofisher
Vienna, Austria
4mo
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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Contractor Senior Clinical Research Associate - Contractor - UK
Worldwide Clinical Trials
UK
4mo
Conducting site qualification, initiation, monitoring, and close-out visits to ensure protocol adherence and data integrity for clinical trials.
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Clinical Research Associate II
Avania
Deutschland
4mo
Establish, maintain, and support clinical trials by verifying subject rights, data accuracy, and protocol compliance through site monitoring.
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Clinical Research Associate - Germany
Linical
Moosach, München
4mo
Manage investigative sites across Germany to ensure clinical trials are conducted in accordance with study protocols, ICH-GCP, and regulatory requirements.
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CRA I/ II- FSP
ThermoFisher Scientific
Madrid
5mo
Conduct remote and on-site clinical monitoring to ensure protocol and regulatory compliance for oncology studies, managing site processes and data reliability.
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Clinical Research Associate
Evolve Scientific
The Rocks, Sydney
5mo
Monitoring clinical trials in ophthalmology for a leading Australian CRO.
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Clinical Research Associate - Italy
Worldwide Clinical Trials
Italia
5mo
Managing research activities at sites for clinical registries and non-interventional/observational studies.
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