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Healthcare
› Clinical Research Associates
Clinical Research Associates
877 open positions
Assistant CRA
Thermofisher
Remote
today
Provide support for site preparedness, logistical monitoring, and remote monitoring activities in clinical trials.
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CRA(Level II)
Thermofisher
Remote, China
today
Conducts remote or on-site clinical monitoring and site management to ensure protocol compliance, data accuracy, and subject safety across global trials.
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CRA(Level II)
Thermofisher
Remote, China
today
Conducts remote or on-site clinical monitoring and site management to ensure protocol compliance, data accuracy, and subject safety across global trials.
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Senior Investigator Services Representative
Iqvia
Singapore
today
Liaise with clinical investigator sites to manage alert values, critical values, data clarifications, and revision requests for active clinical trials.
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Clinical Research Associate II
Msd
ROU - Bucuresti - Bucuresti (Ana Tower), RO
today
Manage assigned clinical trial sites to ensure protocol compliance, data integrity, and patient safety across all study phases.
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Senior Clinical Research Associate
AbbVie
Beijing, Beijing, cn
1d
Senior Clinical Research Associate acting as the primary sponsor point of contact for investigative sites, leading site engagement, training, and monitoring to ensure protocol compliance and patient safety.
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Clinical Research Associate - Experienced II/Sr
Jobgether
Remote
1d
Conduct on-site and remote monitoring visits to clinical trial sites to ensure compliance with protocols, regulations, and quality standards.
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Junior Clinical Research Associate – Transition Opportunity for ACRAs & Junior CRAs
Thermofisher
Brisbane, Australia
1d
Transitioning Clinical Research Coordinators or junior CRAs into a Clinical Research Associate role to perform clinical monitoring and site management.
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Clinical Operations Manager
Iqvia
North Sydney, New South Wales, Australia
1d
Lead, coach, and mentor a team of Clinical Research Associates (CRAs) and Clinical Trial Assistants (CTAs) to ensure high-quality clinical trial delivery and site monitoring.
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CRA I, CRA II and Senior CRA
Icon
Japan, Tokyo
1d
Clinical trial monitoring and study setup coordination to ensure patient safety and regulatory compliance.
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Clinical Research Associate
Icon
Germany, Frankfurt
1d
Deliver clinical trial monitoring work to a high standard, coordinating study setup and monitoring, managing queries, and ensuring patient safety and regulatory compliance.
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Central Review Manager (CRM)
Thermofisher
Mexico City, Mexico
1d
Perform centralized review and approval of clinical monitoring visit reports (PSA, SI IMV, CO) to ensure protocol consistency, site safety, and regulatory compliance across global projects.
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FSP CRA 1 & CRA 2
Iqvia
Lima, Peru
1d
Conduct site monitoring visits and manage clinical trial sites to ensure adherence to study protocols, GCP, and ICH guidelines.
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Clinical Research Associate, Full Service
Iqvia
Durham, North Carolina, United States of America
$75k–$175k
1d
Perform monitoring and site management to ensure clinical studies are conducted per protocol and regulations.
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Clinical Research Associate II (CRA II) - São Paulo, Brasil
Msd
BRA - Sao Paulo - Sao Paulo (Torre Z), BR
1d
Primary site contact for clinical research studies, ensuring protocol compliance and data quality across all trial phases.
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Senior Analytical Monitor
↗
Johnson & Johnson Innovative Medicine
Maidenhead, England, UK
1d
Senior Analytical Monitor executes analytical monitoring activities for clinical trials, using data analytics to identify risks, trends, and early warning signals regarding data quality, participant safety, and compliance to support Site Managers.
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Senior Specialist, Clinical Research Monitoring
Edwards
USA-California-Remote
$108k
1d
Field monitoring of clinical trials to ensure data consistency, safety, and regulatory compliance for medical device studies.
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FSP CRA II
↗
Thermo Fisher Scientific
Bangkok, Bangkok City, Thailand
1d
Clinical Research Associate responsible for site evaluation, monitoring visits, and ensuring study compliance with ICH GCP and local regulations.
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FSP CRA II
Thermofisher
Bangkok, Thailand
2d
Clinical Research Associate responsible for site evaluation, monitoring visits, and ensuring study compliance with ICH GCP and local regulations.
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Risk Manager (Clinical Research)-Poland
Indero
Warsaw, Poland
3d
Develop and execute risk-based monitoring strategies to ensure data quality and integrity in clinical research projects.
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Senior Clinical Research Associate
↗
Mep Health
Overland Park, KS
3d
Conduct independent monitoring for Phase I clinical trials across local research facilities and external investigator sites.
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Clinical Research Associate II
↗
Biospace
Vancouver, WA
3d
Proactively solves study-related clinical site issues to ensure successful protocol execution for Phase I-III clinical studies.
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Spécialiste/associé recherche clinique
↗
Fop Consultants
Remote
3d
Clinical research specialist/associate monitoring clinical studies for (bio)pharmaceutical clients to ensure compliance with operational procedures and regulatory requirements.
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FSP Sr CRA - Medical Device - East Coast
↗
Thermo Fisher Scientific
New York, United States
$89k–$145k
3d
Senior Clinical Research Associate conducting risk-based monitoring, site management, and audit readiness for medical device clinical trials.
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Senior Clinical Research Associate - CNS
↗
Worldwide Clinical Trials
Triangle, NC
$97k–$193k
3d
Manage research activities at clinical trial sites for CNS therapeutic areas, covering study start-up, site training, maintenance, and close-out.
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Clinical Research Associates (CRA)
↗
University of Utah Health Research
Salt Lake City, UT
$60k–$90k
3d
Monitor all aspects of clinical research, conduct on-site visits for site selection and monitoring, and ensure trial activities comply with protocols and regulatory requirements.
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Clinical Research Associate II (GTA)
↗
Biospace
Oakville, MO
3d
Proactively solves study-related clinical site issues and ensures successful protocol-level execution of Clinical Site Management deliverables involving start-up, execution, and close-out of studies.
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Data Surveillance Analyst
↗
Parexel
Hyderabad, Telangana, India
3d
Lead centralized monitoring activities for global clinical trials to ensure data accuracy, patient safety, and regulatory compliance.
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CTC
↗
ICON Strategic Solutions
Sydney, New South Wales, Australia
3d
Support the management of clinical trial sites by assisting with site monitoring activities, ensuring compliance with study protocols, and maintaining high standards of operational efficiency.
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CTM I - only CDMX - Remote
↗
Syneos Health
3d
Clinical Monitoring Associate I performing site qualification, initiation, monitoring, and close-out visits to ensure regulatory compliance and data integrity for clinical trials.
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Single Sponsor UK Senior CRA II - South West Region (Must have solid UK monitoring exp)
↗
Syneos Health
3d
Senior Clinical Research Associate performing site qualification, monitoring, and site management to ensure regulatory compliance and data integrity for clinical trials.
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Single Sponsor CRA I / II (Must have UK monitoring exp)
↗
Syneos Health
3d
Clinical Research Associate performing site qualification, monitoring, and site management for clinical trials to ensure regulatory compliance and data integrity.
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Centralized Monitor
Ergomed
Sarajevo, ba
4d
Reviews and analyzes centralized clinical trial data to identify risk signals, monitor site performance, and ensure protocol compliance.
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Centralized Monitor
Ergomed
Belgrade, rs
4d
Performs review and analysis of centralized, aggregated data to identify potential signals and trends in predefined risk indicators for clinical studies.
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Senior Clinical Research Associate
AbbVie
Taipei, tw
4d
Ensure successful protocol level execution of SMM deliverables involving start-up, execution, and close-out of clinical studies.
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Clinical Research Associate II
Psi-Cro
Barcelona, CT, es
4d
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 II
Jobgether
Brazil
4d
Conduct on-site clinical monitoring visits, support study startup, and ensure clinical research quality across Phase II/III trials.
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Senior Clinical Research Associate
Jobgether
Brazil
4d
Senior Clinical Research Associate overseeing site-level activities, mentoring junior CRAs, and ensuring regulatory compliance and study execution across complex clinical trials.
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Clinical Research Associate
Icon
Georgia, US
4d
Conduct clinical trial monitoring activities including site qualification, initiation, monitoring, and close-out visits for cardio and obesity trials.
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Senior Clinical Research Associate (Sr. CRA)
↗
Clinixir
Bangkok City, Thailand
4d
Monitor and manage Phase I-IV clinical research projects at investigative sites to ensure compliance with protocols, SOPs, and ICH-GCP regulations.
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Senior Clinical Research Associate - Core Team
↗
Parexel
4d
Senior Clinical Research Associate responsible for end-to-end site management, ensuring protocol adherence, data integrity, and regulatory compliance for oncology clinical trials.
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Clinical Research Associate II
↗
Psi Cro
Barcelona, Catalonia, Spain
4d
Conduct onsite monitoring visits, manage study startup, and ensure data compliance and subject safety across various therapeutic indications.
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Clinical Research Associate
Thermofisher
Milan, Italy
4d
Coordinate clinical monitoring and site management to ensure protocol and regulatory compliance across global trials.
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Sr CRA (Level II)
Thermofisher
Guangdong, China
4d
Conducts remote and 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 I - Sponsor dedicated - Netherlands - Home based (m/w/d)
Iqvia
Amsterdam, Netherlands
4d
Conduct site qualification, initiation, monitoring, and close-out visits to ensure patient safety, data integrity, and protocol compliance across clinical trials.
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Senior Clinical Research Associate - Sponsor dedicated - Belgium - Home based (m/w/d)
Iqvia
Zaventem, Belgium
€4k
4d
Conduct site qualification, initiation, monitoring, and close-out visits to ensure patient safety, data integrity, and protocol compliance for clinical research programs.
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Senior Clinical Research Associate
Novartis
Remote
$109k–$202k
4d
Manage trusted site relationships and perform on-site and remote monitoring activities to support the initiation, conduct, and timely completion of Phase I – IV clinical trials.
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Clinical Research Associate - Cross Therapeutic Area
Icon
Denver, CO, US
$91k–$114k
4d
Primary liaison between investigational sites and the sponsor, conducting site visits (selection, initiation, routine monitoring, close-out) to ensure compliance and data quality.
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Senior CRA
↗
ICON Strategic Solutions
Atlanta, GA
4d
Oversee and manage clinical trial activities for ophthalmology studies, ensuring adherence to protocols, regulatory requirements, and GCP standards.
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CRA risk-based monitoring
↗
Syneos Health
4d
Conduct risk-based monitoring visits (on-site or remote) to ensure regulatory compliance, data integrity, and patient safety across clinical study sites.
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