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Healthcare
› Clinical Research Associates
Clinical Research Associates
701 open positions
Site Care Partner - FSP
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Parexel
Remote
5mo
Manage clinical trial sites for oncology studies, handling start-up, activation, recruitment, and close-out to ensure site readiness and enrollment targets.
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Clinical Research Associate II (CRA II) – FSP Business Unit
Thermofisher
Remote, Romania
6mo
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, Single Sponsor dedicated in Poland
Iqvia
Warszawa, mazowieckie
6mo
Performing monitoring and site management work to ensure clinical trial sites conduct studies and report data per protocol and regulations.
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In-House Clinical Research Associate (Poland)
Alimentiv
Warszawa, mazowieckie
6mo
Required skills: Undergraduate university degree (Bachelor or Honors Bachelor), 1-3 years' related experience Responsibilities: Support and observe clinical site monitoring services inhouse, provide monitoring and site management activities, assess for…
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CRA (Level II)
Thermo Fisher Scientific
Remote
6mo
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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CRA I/II/ Sr CRA - FSP - UK
Thermo Fisher Scientific
UK
6mo
Conduct independent on-site clinical monitoring to ensure data quality and regulatory compliance for pharmaceutical clinical trials.
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CRA I/II/ Sr CRA - FSP - UK
ThermoFisher Scientific
UK
6mo
Conduct independent on-site clinical monitoring to ensure data quality and regulatory compliance for pharmaceutical clinical trials.
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Director - DDC
Novotech
Melbourne CBD, Melbourne
6mo
Ensuring rights and wellbeing of trial participants are protected and reported trial data are accurate, complete, and verifiable from source documents.
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Experienced CRA
Thermofisher
Stockholm, Sweden
6mo
Senior Clinical Research Associate conducting risk-based monitoring of clinical trial sites across Sweden, Norway, and Finland to ensure protocol compliance and data reliability.
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CRA I/II - FSP - UK - Vaccines
Thermo Fisher Scientific
UK
7mo
Conduct independent on-site clinical monitoring for vaccine and oncology studies to ensure data quality and regulatory compliance.
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CRA I/II - FSP - UK - Vaccines
ThermoFisher Scientific
UK
7mo
Conduct independent on-site clinical monitoring for vaccine and oncology studies to ensure data quality and regulatory compliance.
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CRA I/CRA II (m/f/d) - FSP Germany
ThermoFisher Scientific
Deutschland
7mo
Managing clinical trial sites across Germany to ensure compliance with protocols, ICH-GCP, and regulations.
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Senior CRA (Sponsor dedicated)
ICON Clinical Research
Frankfurt am Main, Hessen
7mo
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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CRA I/CRA II/Sr CRA
Thermofisher
Singapore, Singapore
7mo
Conduct remote or on-site clinical monitoring visits to assess protocol and regulatory compliance, manage documentation, and ensure data reliability across clinical trials.
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CRA single-sponsor in Germany Diabetes and Obesity
Syneos Health
Deutschland
7mo
Clinical Research Associate performing site qualification, initiation, monitoring, and close-out visits for Diabetes and Obesity clinical trials in Germany.
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Senior CRA I/II - Senior Klinischer Monitor (m/w/d)
ThermoFisher Scientific
Remote
7mo
Manage clinical trial sites across Germany ensuring compliance with protocol, ICH-GCP, and regulations using a risk-based monitoring approach.
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Senior CRA I/II - Senior Klinischer Monitor (m/w/d)
Thermo Fisher Scientific
Deutschland
7mo
Managing clinical trial sites across Germany to ensure compliance with protocols, ICH-GCP, and regulations through risk-based monitoring.
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Principal CRA – Lead Monitor (m/w/d)
Thermo Fisher Scientific
Deutschland
7mo
Lead and coordinate clinical monitoring and site management for complex, high-risk clinical trials across multiple sponsor models, ensuring compliance with ICH-GCP and EU regulations.
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CRA (Level II)
Thermofisher
Beijing, China
7mo
Conducts remote or on-site clinical monitoring and site management to ensure protocol and regulatory compliance, guaranteeing subject rights and data reliability.
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Clinical Research Associate II / Senior Clinical Research Associate Large Pharma
Ire
Frankfurt am Main, Hessen
7mo
Overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) standards, ensuring data integrity and participant safety.
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CRA 2
ICON Clinical Research
Madrid
8mo
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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Sr/CRA I/II - UK (numerous locations)
Thermo Fisher Scientific
UK
8mo
Conducts remote and on-site monitoring of clinical trial investigator sites to ensure protocol and regulatory compliance, data accuracy, and subject safety.
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Clinical Research Associate/Senior Clinical Research Associate- FSP
Parexel
Annapolis, Anne Arundel County
8mo
Managing clinical trial sites to ensure study conduct compliance with ICH-GCP and local regulations, overseeing site initiation, monitoring, and closure for oncology and cell therapy studies.
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Senior Clinical Research Associate (Netherlands)
WEP Clinical
Remote, Netherlands
8mo
Oversees clinical monitoring and site management to ensure protocol adherence, data accuracy, and regulatory compliance for clinical trials.
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Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane
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Thermo Fisher Scientific
Remote
8mo
Conduct clinical monitoring and site management for sponsor-driven trials, ensuring protocol and regulatory compliance.
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CRA - FSP - Central Poland
Thermo Fisher Scientific
Remote
8mo
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 - FSP - Central Poland
ThermoFisher Scientific
Warszawa, mazowieckie
8mo
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 II/Sr CRA - Sponsor-Dedicated FSP - Germany (m/f/d)
Thermo Fisher Scientific
Deutschland
8mo
Manage clinical trial sites across Germany to ensure studies are conducted in compliance with protocol, ICH-GCP, and regulations.
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CRA II/Sr CRA - Sponsor-Dedicated FSP - Germany (m/f/d)
ThermoFisher Scientific
Deutschland
8mo
Managing clinical trial sites across Germany to ensure compliance with protocols, ICH-GCP, and regulations while delivering high-quality, inspection-ready trials.
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Sr/CRA I/II - UK (numerous locations)
ThermoFisher Scientific
UK
8mo
Conducting clinical monitoring and site management for pharmaceutical trials to ensure protocol compliance, data accuracy, and subject safety.
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Join our Talent Pool - Clinical Research Associates (Europe)
Alimentiv
Deutschland
8mo
Proactive recruitment for Clinical Research Associates to support site management, data quality, and regulatory compliance across the study lifecycle.
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Join our Talent Pool - Clinical Research Associates (Canada)
Alimentiv
London, Ontario
9mo
Proactively inviting qualified candidates to join a talent pool for anticipated Clinical Research Associate needs to support the Clinical Monitoring team.
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Clinical Research Associate II / Senior Clinical Research Associate Biotech
Ire
Frankfurt am Main, Hessen
9mo
Overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) standards, ensuring data integrity and participant safety.
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Clinical Research Associate (CRA) (m/w/d) – Zelltherapie (Außendienst)
AstraZeneca
Germany - Hessen
9mo
Monitoring clinical trials in cell therapy (e.g., CAR-T, TCR-T, Treg) to ensure data integrity, document submission, and patient safety across all study phases.
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Clinical Research Associate
Alexion
München, München (Kreis)
10mo
Ensuring delivery and compliance of clinical studies at assigned sites through monitoring, data review, and site management.
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CRA II
Icon
España
10mo
Coordinate clinical monitoring and site management for Phase I-IV trials, ensuring protocol adherence, patient safety, and data integrity across multiple therapeutic areas.
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Clinical Research Associate II/I
Psi-Cro
Shanghai, Beijing, cn
10mo
Conduct on-site monitoring visits, review case report forms, verify source documents, and manage clinical study sites in China.
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Junior Clinical Research Associate (CRA) – Transition Opportunity for CRCs & Junior CRAs | Brisbane
Thermo Fisher Scientific
Australia
12mo
Conduct on-site and remote clinical monitoring visits to ensure protocol and regulatory compliance, manage site documentation, and verify source data for clinical trials.
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Junior Clinical Research Associate (CRA) - Transition Opportunity for CRCs & Junior CRAs | Brisbane
ThermoFisher Scientific
Brisbane, Brisbane Region
12mo
Monitor clinical trials at investigational sites to ensure protocol and regulatory compliance, manage site documentation, and verify source data.
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Clinical Research Associate / Klinischer Monitor (m/w/d)
Iges GMBH
Remote
1y
Monitoring clinical trials for pharmaceuticals, medical devices, and digital health applications across Europe.
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Senior Clinical Research Associate
WEP Clinical
Remote, US
1y
Oversees clinical monitoring and site management to ensure protocol adherence, data accuracy, and regulatory compliance for clinical trials.
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Clinical Research Associate II and Senior Clinical Research Associate
ClinChoice
Veldhoven, Noord-Brabant
1y
Manage clinical study activities across multiple sites for medical devices, overseeing site performance and ensuring high-quality deliverables through monitoring.
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Clinical Site Manager
Icon
España
1y
Partnering with a pharmaceutical company to monitor multiple Phase I-IV clinical trial sites and build strong relationships with investigators and study coordinators to ensure high-quality trial conduct.
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CRA - Multi Sponsor
Icon
Madrid
1y
Overseeing and managing clinical trial activities to ensure adherence to protocols, regulatory requirements, and Good Clinical Practice (GCP) standards while ensuring data integrity and participant safety.
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인재풀 - CRA (Home-based/Hybrid, 상시모집)
Thermofisher
Remote
1y
Clinical Research Associate (CRA) supporting end-to-end clinical trials including site monitoring, data verification, and study closeout for commercial and government contracts.
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SENIOR SITE MANAGER
Jj
Warsaw, Masovian, Poland
1y
Primary contact between Sponsor and Investigational Site ensuring inspection readiness and compliance with clinical trial protocols, SOPs, and GCP from start-up to closure.
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Hong Kong FSP CRA
Thermofisher
Kwai Chung, Hong Kong, China
1y
Performs and coordinates clinical monitoring and site management for investigational sites to ensure protocol compliance, data accuracy, and subject safety.
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Clinical Operations Lead (Clinical Trial Manager)
Alimentiv
Deutschland
1y
Required skills: Oversight of project deliverables, assigned Clinical Research Associates (CRAs) and Investigator sites in accordance with the Monitoring Plan, Protocol, Good Clinical Practice (GCP), ICH guidelines and local regulations.
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Clinical Operations Lead
Alimentiv
Remote
1y
Oversees clinical operations for a project, managing CRAs and investigator sites to ensure compliance with protocols, GCP, and regulations.
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CRA (Level II)
Thermofisher
Shanghai, China
2y
Performs clinical monitoring and site management to ensure protocol compliance, data accuracy, and regulatory adherence for global medical research trials.
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