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Healthcare
› Clinical Research Associates
Clinical Research Associates
883 open positions
Senior Clinical Research Associate
AbbVie
Seoul, Seoul, kr
3mo
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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Clinical Research Associate - FSP - Czechia
Thermofisher
Remote, Czechia
3mo
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
3mo
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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Clinical Research Associate - Cross TA
↗
ICON Strategic Solutions
Georgia, United States
3mo
Primary liaison between investigational sites and the sponsor, conducting site visits (selection, initiation, monitoring, close-out) to ensure compliance and data quality.
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FSP CRA (Level II)
Thermofisher
Remote, Mexico
3mo
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
↗
ICON Strategic Solutions
Bengaluru, Karnataka, India
3mo
Conducting site qualification, initiation, monitoring, and close-out visits for Phase II & III Oncology clinical trials to ensure protocol compliance, data integrity, and patient safety.
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FSP CRA(Level II)
Thermofisher
Chengdu, China
3mo
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 Levels II/Sr - FSP - Portugal
Thermofisher
Remote, Portugal
3mo
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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Clinical Research Associate II
Psi-Cro
Remote, US, us
3mo
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
3mo
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
3mo
Conducting clinical monitoring visits, training site staff, and managing complex clinical studies to ensure data quality and regulatory compliance.
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Sr. CRA 3, Brazil, IQVIA Biotech
Iqvia
Brasil
3mo
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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Experienced Clinical Research Associate (Remote, Guangzhou)
Medpace
Remote
3mo
Full-time, home-based Clinical Research Associate supporting drug development from feasibility to closeout across Phase 1-3 trials.
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Clinical Research Associate
Ire
São Paulo, Estado de São Paulo
3mo
Conduct clinical trial monitoring to ensure study compliance, patient safety, and data accuracy across clinical programmes.
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Clinical Trial Site Relationship Coordinator (Finnish Speaking)
↗
Medpace
London, England, UK
3mo
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 Clinical Research Associate - Sponsor Dedicated - Oncology Experience Needed
↗
Parexel
Uxbridge, England, UK
3mo
Manage assigned clinical trial investigator sites from activation through database lock, ensuring patient safety and quality study execution.
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Experienced Clinical Research Associate (Remote, Wuhan)
Medpace
China
3mo
Conduct feasibility, pre-study, initiation, monitoring, and closeout visits for research sites in Phase 1-3 clinical trials across various therapeutic areas.
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Clinical Research Associate (CRA) - Dallas
↗
Medpace
Irving, TX
3mo
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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Entry Level - Clinical Research Associate
↗
Medpace
London, England, UK
3mo
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 Site Relationship Coordinator
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Medpace
South Yarra, Victoria, Australia
3mo
Full-time office-based role managing strategic relationships with clinical research sites to support study feasibility, selection, and start-up activities in Australia.
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Clinical Research Associate - Clinical Research Coordinator Experience
↗
Medpace
Cincinnati, OH
3mo
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
3mo
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)
↗
Medpace
Phoenix, AZ
3mo
Conduct qualification, initiation, monitoring, and closeout visits at research sites to ensure compliance with protocols and regulations.
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Clinical Research Associate (Home-based, Adelaide)
↗
Medpace
Adelaide, South Australia, Australia
3mo
Conduct on-site monitoring visits for clinical research sites to ensure compliance with protocols and regulatory requirements.
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Clinical Research Associate (Home-based, Brisbane)
↗
Medpace
Brisbane, Queensland, Australia
3mo
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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Experienced CRA Manager
↗
Medpace
Munich, Bavaria, Germany
3mo
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
3mo
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
3mo
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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Clinical Research Associate - Entry (Beijing)
Medpace
Beijing, China
4mo
Conduct qualification, initiation, monitoring, and closeout visits for clinical research sites to ensure compliance with protocols and regulations.
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CRA II
↗
Fortrea
Maidenhead, England, UK
4mo
Lead and manage clinical trial sites across diverse and complex therapeutic areas including oncology, neuroscience, and cell & gene therapy.
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Centralized Clinical Trial Manager
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ICON Plc
Bengaluru, Karnataka, India
4mo
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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Clinical Research Associate II - Sydney
↗
Fortrea
Sydney, New South Wales, Australia
4mo
Managing and monitoring clinical trials to ensure compliance with regulatory requirements and data integrity while fostering relationships with investigative sites.
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Clinical Research Associate
Bms
Otemachi-JP
4mo
Monitor clinical trial progress and ensure compliance with protocols, SOPs, GCP, and regulations across multiple sites and therapeutic areas.
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Clinical Operations Lead (Tokyo or Osaka)
Psi-Cro
Tokyo, Tokyo, jp
4mo
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
4mo
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
4mo
Supports Clinical Research Associates with remote monitoring, site preparedness, logistics, and document management to ensure high-quality clinical trial execution.
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Clinical Research Associate
Medpace
Milan, Italy
€29k
4mo
Conduct on-site monitoring visits at clinical research sites to ensure compliance with protocols, GCP, and regulatory requirements for drug and medical device development.
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CRA II - Saudi Arabia
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 clinical trials.
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CRA Manager
Msd
MYS - Selangor - Petaling Jaya (Ascent Paradigm)
4mo
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
4mo
Independently performs, coordinates, and oversees all aspects of clinical site monitoring services, assessing protocol and regulatory compliance for clinical studies.
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Experienced CRA (multi-sponsor, multi-therapeutic, home-based and office-based positions available)
↗
Medpace
4mo
Conducting clinical monitoring visits at research sites to ensure protocol compliance, data accuracy, and patient safety across various therapeutic areas.
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CRA I - Senior CRA (FSP)
Thermofisher
Remote
4mo
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 Operations Lead (Clinical Trial Manager)
Alimentiv
Frankfurt
4mo
Oversees clinical operations for a project at a regional or global level, managing deliverables, CRAs, and Investigator sites.
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Site and Monitoring Health Lead - FSP
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Parexel
Remote
5mo
Lead oversight of clinical trial execution at investigator sites to safeguard quality and ensure CRO monitoring effectiveness.
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Clinical Research Associate I/II - Core Team
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Parexel
Remote
5mo
Act as Parexel's direct contact with assigned clinical sites to ensure study integrity, protocol adherence, and compliance from initiation through close out.
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Senior Clinical Research Associate - FSP
↗
Parexel
Remote, US
5mo
Ensure proper conduct of clinical trials in accordance with Study Monitoring Plan, GCP, and client standards to achieve project goals, timelines, and quality.
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Experienced Clinical Research Associate
Medpace
Taipei, Taiwan
5mo
Conduct on-site monitoring visits for clinical research sites to ensure compliance with protocols, GCP, and regulatory requirements for drug and medical device development.
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Clinical Research Associate - Entry
Medpace
Taipei, Taiwan
5mo
Conduct on-site monitoring visits for clinical research sites to ensure compliance with protocols, GCP, and regulatory requirements for drug and medical device development.
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Sr/CRA I/II - UK (numerous locations)
Thermofisher
Remote, United Kingdom
5mo
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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Part-Time CRA II - Klinischer Monitor (0.8 FTE) (m/w/d)
Thermofisher
Remote
5mo
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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