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Healthcare
› Clinical Research Associates
Clinical Research Associates
553 open positions
Clinical Research Associate I (FSP)
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Thermo Fisher Scientific
Melbourne, VIC, AU
27d
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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サ
Site Care Partner (Sponsor dedicated) - Buenos Aires only - Min 6+ years of previous monitoring experience, ideally in Oncology!
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サイネオス・ヘルス
Desde casa, AR
27d
Senior Clinical Research Associate (Site Care Partner) responsible for site qualification, monitoring, management, and close-out visits to ensure regulatory compliance and data integrity in clinical trials.
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Clinical Research Associate I (FSP)
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Thermo Fisher Scientific
Sydney, NSW, AU
27d
Conduct remote and on-site clinical monitoring and site management to ensure protocol and regulatory compliance for clinical trials.
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Assistant CRA
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Thermo Fisher Scientific
Remote
27d
Provide administrative and logistical support for clinical trial site management and remote monitoring activities.
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Site Care Partner (Sponsor dedicated) - Buenos Aires only - Min 6+ years of previous monitoring experience, ideally in Oncology!
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Syneos Health
Desde casa, AR
27d
Senior Clinical Research Associate (Site Care Partner) responsible for site qualification, monitoring, management, and close-out visits to ensure regulatory compliance and data integrity in clinical trials.
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Clinical Research Associate I (FSP)
Thermofisher
Remote
27d
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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CRA I/II/ Sr CRA - FSP - UK
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Thermo Fisher Scientific
Remote, GB
27d
Conduct independent on-site clinical monitoring to ensure trial quality and accuracy across multi-national projects.
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Sr Clinical Research Associate FSP
Thermo-Fisher-Scientific
Melbourne, Victoria
27d
Senior Clinical Research Associate conducting risk-based monitoring, site management, and compliance assurance for clinical trials.
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Clinical Research Associate II
Psi-Cro
Tokyo/Osaka, jp
27d
Manage clinical aspects of full-service global projects in Japan, ensuring timelines, targets, and standards while building relationships with clinical sites and investigators.
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Senior Clinical Research Associate
Psi-Cro
Tokyo/Osaka, jp
27d
Conduct site monitoring, initiation, and close-out visits for clinical studies in various therapeutic areas to ensure data quality and regulatory compliance.
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Site Care Partner
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ICON Plc
Blue Bell, PA, US
28d
Foster relationships with clinical trial sites to enhance engagement and support the advancement of innovative treatments.
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Clinical Research Associate II
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Psi Cro
Remote
28d
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
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Pfizer
New York, NY, US
$69k–$69k
28d
Manage investigator sites for clinical trials to ensure patient safety, quality execution, and compliance with GCP and Pfizer standards.
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Clinical Research Associate
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Beone Medicines
En remoto, ES
$46k–$46k
28d
Executes clinical monitoring activities at trial sites to ensure data quality and regulatory compliance for oncology/hematology clinical trials.
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Senior Clinical Research Associate I
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Pfizer
New York, NY, US
$83k–$83k
28d
Manage investigator sites for clinical trials to ensure patient safety, quality study execution, and compliance with GCP and company standards.
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Senior Clinical Research Associate II
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Pfizer
New York, NY, US
$99k–$99k
28d
Manage investigator sites for clinical trials to ensure patient safety, quality execution, and compliance with GCP and Pfizer standards.
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Clinical Lead (Lead Clinical Research Associate)
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Avania
Remote
$145k–$145k
28d
Lead Clinical Research Associate supervising monitoring activities for medical device and MedTech studies to ensure ethical and clinical standards.
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Senior Clinical Research Associate - UK - CNS/Oncology - Remote
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Worldwide Clinical Trials
Remote
28d
Managing research activities at sites for clinical research projects, predominantly registries and non-interventional/observational studies in CNS and Oncology.
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Assistant CRA
Thermofisher
Remote
28d
Support Clinical Research Associates (CRAs) with site preparedness, logistical monitoring, and administrative tasks to ensure compliance with regulatory guidelines.
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Sr. Clinical Research Associate
AbbVie
Shanghai, Shanghai, cn
29d
Senior Clinical Research Associate acting as the primary sponsor point of contact for investigative sites, leading site engagement, monitoring, and risk management to ensure protocol compliance and patient safety.
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CRA (Level II) to Sr CRA (Level II)
Thermofisher
Madrid, Spain
29d
Conduct remote and on-site clinical monitoring visits to assess protocol and regulatory compliance, manage documentation, and ensure data accuracy for pharmaceutical clinical trials.
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サ
CTM I/II
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サイネオス・ヘルス
Remote
29d
Oversees site management, clinical monitoring, and central monitoring deliverables to ensure patient safety, protocol compliance, and data integrity across clinical trials.
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Clinical Research Associate
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ICON Plc
Reading, ENG, GB
29d
Overseeing clinical trial site performance, ensuring data quality and patient safety for oncology studies.
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Clinical Research Associate
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ICON Plc
Sydney, NSW, AU
29d
Design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies.
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Senior Clinical Research Associate (SCRA)
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Beone Medicines
Remote, AU
29d
Managing and overseeing clinical trials to ensure compliance with GCP, ICH guidelines, and local regulations while safeguarding participant safety.
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Clinical Trial Manager II, Dermatology & Rheumatology CRO, Australia
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Indero
Remote, AU
29d
Operational management and oversight of clinical investigative sites and clinical monitoring deliverables for clinical trials in Dermatology and Rheumatology.
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Assistant CRA
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Thermo Fisher Scientific
Remote, GB
29d
Supports Clinical Research Associates with remote monitoring, site preparedness, logistics, and document management for clinical trials.
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Quality Manager, Clinical
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Iqvia
Valencia, CA, US
$63k–$63k
29d
Ensure clinical trial compliance and quality across designated delivery units by overseeing site assessments, managing CAPAs, and driving inspection readiness.
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Senior CRA
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ICON Plc
Raleigh, NC, US
$111k–$111k
29d
Monitoring clinical trial sites in oncology to ensure adherence to study protocols, regulatory requirements, and GCP standards.
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Join our Talent Pool - Sr Clinical Research Associate (Portugal)
Alimentiv
Lisboa
29d
Senior Clinical Research Associate providing site monitoring, study management, and mentorship for clinical trials across Portugal and Spain.
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Senior Clinical Research Associate
Psi-Cro
Remote
29d
Conducting onsite monitoring visits, reviewing clinical data, and ensuring subject safety and data compliance for Phase II and III clinical trials.
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サ
Clinical Research Associate (CRA) II (remote, Client based)
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サイネオス・ヘルス
Remote
1mo
Conducts on-site and remote clinical monitoring activities to ensure regulatory compliance and data integrity across the drug development lifecycle.
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サ
Clinical Research Associate (CRA) II (remote, Client based)
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サイネオス・ヘルス
Remote
1mo
Conducts on-site and remote clinical monitoring activities to ensure regulatory compliance and data integrity across the drug development lifecycle.
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Clinical Research Associate 1 or 2 (m/w/d), Multi-Sponsor, Germany
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Iqvia
Remote
1mo
Conduct monitoring on complex clinical trials for various pharma companies to assure adherence to GCP and study protocols.
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Clinical Research Associate
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ICON Plc
US
1mo
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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Site Care Partner
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ICON Plc
Blue Bell, PA, US
1mo
Foster relationships with clinical trial sites to enhance engagement and support the advancement of innovative treatments.
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SMA II
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ICON Plc
Blue Bell, PA, US
1mo
Support the management and monitoring of clinical trial sites to ensure compliance with study protocols, regulatory requirements, and GCP guidelines.
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Clinical Research Associate
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Primedge Workforce Solutions
DL, IN
$360k–$360k
1mo
Conducting clinical trial monitoring activities including site selection, initiation, close-out visits, and ensuring data integrity and protocol adherence.
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Senior Clinical Research Associate/Clinical Research Associate-II
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Prorelix Research
MH, IN
$3600k–$3600k
1mo
Oversee clinical trial execution ensuring protocol compliance, patient safety, data quality, and site performance.
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Lead CRA
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ICON Plc
Blue Bell, PA, US
1mo
Leading site management activities for ophthalmology and gene therapy clinical trials, ensuring compliance with protocols and regulatory guidelines.
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Clinical Trial Coordinator
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ICON Plc
Sydney, NSW, AU
1mo
Support clinical trial site management by assisting with monitoring activities, ensuring protocol compliance, and maintaining operational efficiency.
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Regional Clinical Compliance Manager
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Beone Medicines
Remote
1mo
Ensures GCP compliance and inspection readiness for oncology clinical trials across Brazil, managing site visits and risk assessments.
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サ
FSP- Sr CRA I/ II
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サイネオス・ヘルス
Remote
1mo
Conduct on-site and remote monitoring of clinical research studies to ensure compliance with clinical practices and regulations.
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Clinical Research Associate (CRA) II (remote, Client based)
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Syneos Health
Remote
1mo
Conducts on-site and remote clinical monitoring activities to ensure regulatory compliance and data integrity across the drug development lifecycle.
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サ
CRA II- FSP
↗
サイネオス・ヘルス
Remote
1mo
Clinical Research Associate performing site qualification, monitoring, and management to ensure regulatory compliance and data integrity in clinical trials.
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Senior Clinical Research Associate/ Clinical Research Associate II
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Precision for Medicine
Remote
1mo
Monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocol, SOPs, ICH-GCP, and regulations.
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CRA II- FSP
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Syneos Health
Remote, AU
1mo
Clinical Research Associate performing site qualification, monitoring, and management for clinical trials in the life sciences industry.
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CRA II- FSP
↗
Syneos Health
Remote, AU
1mo
Clinical Research Associate performing site qualification, monitoring, and management to ensure regulatory compliance and data integrity for clinical trials.
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CRA II- FSP
↗
Syneos Health
Remote, AU
1mo
Clinical Research Associate performing site qualification, monitoring, and management to ensure regulatory compliance and data integrity for clinical studies.
♥
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サ
CRA II- FSP
↗
サイネオス・ヘルス
Remote
1mo
Clinical Research Associate performing site qualification, monitoring, and management to ensure regulatory compliance and data integrity for clinical trials.
♥
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