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Healthcare
› Clinical Research Associates
Clinical Research Associates
548 open positions
CRC III
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Dynamed Clinical Research Lp
Tomball, TX, US
20d
Ensure quality research and data collection at assigned clinical trial sites in accordance with sponsor protocols, FDA regulations, and ICH/GCP guidelines.
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Clinical Research Associate
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Orca Bio
Remote, US
20d
Monitor clinical trials for blood cancer cell therapies at investigative sites to ensure compliance with protocols and regulations.
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CRA II (Oncology), Full Service, Thailand (remote)
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Syneos Health
Remote
20d
Clinical Research Associate performing site qualification, monitoring, and management for oncology clinical trials in Thailand.
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Experienced CRA II/Sr CRA - US Northeast Region - Multiple Therapeutic Areas Available
Thermofisher
Remote, Massachusetts, USA
$85k–$85k
20d
Conduct remote or on-site clinical monitoring visits to assess protocol and regulatory compliance, manage documentation, and ensure audit readiness for clinical trials.
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(Sr) Clinical Research Associate - Netherlands
Thermofisher
Remote
20d
Conduct independent clinical monitoring and site management for pharmaceutical trials, ensuring protocol and regulatory compliance through on-site and remote activities.
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GCP Auditor (Freelance)
Ergomed
Remote
20d
Planning, conducting, and reporting Good Clinical Practice (GCP) audits for pharmaceutical and biotechnology companies to ensure regulatory compliance and patient safety.
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Senior Clinical Research Associate
Worldwide Clinical Trials
Brasil
20d
Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits to ensure data quality and regulatory compliance.
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Clinical Research Associate II
Thermo-Fisher-Scientific
Sydney, New South Wales
20d
Coordinate clinical monitoring and site management to ensure protocol and regulatory compliance across pharmaceutical and biotech clinical trials.
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In-House Clinical Research Associate
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The Emmes Company, LLC
Remote
21d
Assist with operational activities supporting site management and monitoring of clinical studies/trials, ensuring compliance with protocols and regulatory requirements.
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In-House Clinical Research Associate (Contract)
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4d Molecular Therapeutics
Emeryville, CA, US
$125k–$125k
21d
In-house Clinical Research Associate supporting Phase 3 clinical trial execution, site management, and regulatory compliance for late-stage biotech therapeutics.
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サ
CRA II (Oncology), Full Service, Thailand (remote)
↗
サイネオス・ヘルス
Remote
21d
Clinical Research Associate II performing site qualification, monitoring, and management for oncology clinical trials in Thailand.
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(Sr) Clinical Research Associate - Client-dedicated FSP - Belgium
Thermofisher
Remote
21d
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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(Sr) Clinical Research Associate - Belgium
Thermofisher
Remote
21d
Senior Clinical Research Associate conducting remote and on-site monitoring of investigator sites to ensure protocol and regulatory compliance, manage documentation, and guarantee data reliability for clinical trials.
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(Sr) Clinical Research Associate - Client-dedicated (FSP) Netherlands
Thermofisher
Remote
21d
Conduct remote and on-site clinical monitoring and site management to ensure protocol and regulatory compliance for pharmaceutical clinical trials.
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Senior Clinical Research Associate - West Coast/Oncology
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Systimmune
Remote
$110k–$110k
21d
Manage and oversee clinical study sites for oncology trials to ensure data quality and patient safety in accordance with ICH-GCP guidelines.
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Clinical Research Associate II (FSP) - Melbourne
Fortrea
Melbourne, Victoria
21d
Manage and monitor clinical trials for sponsors, ensuring regulatory compliance, data integrity, and subject protection across investigative sites.
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Clinical Research Associate II (Contract based)
Psi-Cro
Lisbon, Lisbon, pt
21d
Conduct onsite monitoring visits, manage clinical sites, and ensure data compliance for Phase II/III clinical research projects in Inflammatory Bowel Diseases.
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Senior Clinical Research Associate
AbbVie
Minato City, Tokyo, jp
22d
Primary Sponsor point of contact for investigative sites, ensuring appropriate trial conduct, data integrity, and compliance while driving patient recruitment and retention.
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FSP CRA (Level II)
Thermofisher
Guangzhou, China
22d
Monitors clinical trial investigator sites using a risk-based approach to ensure compliance with protocols and regulations, verify data accuracy, and resolve site deficiencies.
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CRA Manager
Msd
PHL - National Capital Region - Makati, PH
22d
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 CRA (Level I)
Thermofisher
Sofia, Bulgaria
22d
Senior Clinical Research Associate conducting remote and on-site monitoring of clinical trial sites to ensure protocol and regulatory compliance.
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Sr. CRA II - General Medicine - East Coast or Mid-West
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Fortrea
Remote, US
$0k–$140k
23d
Lead and support clinical trial monitoring for general medicine studies, ensuring patient safety, data integrity, and protocol adherence across study sites.
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Senior Clinical Research Associate (Midwest)
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Novartis
Remote, US
$109k–$109k
23d
Field-based Senior Clinical Research Associate supporting key accounts in an assigned geography to deliver high-quality clinical trials.
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FSP CRA I & CRA II - Respiratory & Cardiovascular - Southeast region
Thermofisher
Remote, Florida, USA
23d
Conduct remote or on-site clinical monitoring and site management to ensure trials comply with protocols, ICH-GCP guidelines, and regulations for Respiratory and Cardiovascular studies.
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Sr CRA level I
Thermofisher
Remote, Argentina
23d
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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Experienced Clinical Research Associate (CRA II / SR CRA)- Bilingual - US Southeast region - Multiple Therapeutic Areas Available
Thermofisher
Remote, Georgia, USA
23d
Conduct remote and on-site clinical monitoring visits to assess protocol and regulatory compliance, manage documentation, and ensure audit readiness for clinical trials.
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Assistant CRA
Thermofisher
Remote
23d
Support Clinical Research Associates (CRAs) with site preparedness, logistical monitoring, and administrative tasks to ensure clinical trial compliance and data integrity.
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CRA (Level 1)
Thermofisher
Remote, Hungary
23d
Conduct remote and on-site clinical monitoring visits to assess protocol and regulatory compliance, manage site processes, and ensure data reliability for clinical trials.
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In-House Clinical Research Associate
↗
Terumo Aortic
Inchinnan, SCT, GB
23d
Oversee remote site management, centralized monitoring, and data review to ensure compliant delivery of clinical trials.
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CRA Autria
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Syneos Health
Home Office, AT
23d
Clinical Research Associate responsible for site qualification, monitoring, and management of clinical trials in Austria to ensure regulatory compliance and data integrity.
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Central Monitoring Manager
Psi-Cro
Munich, BY, de
23d
Lead the implementation of risk-based monitoring (RBM) approaches for clinical studies to ensure patient safety and data integrity.
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Clinical Research Associate II/III VIC
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Novotech
AU
24d
Monitor clinical trial sites to ensure safety, ethical conduct, and data integrity while driving patient recruitment and site performance.
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Clinical Research Associate II
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Iqvia
Reading, ENG, GB
24d
Conduct on-site monitoring visits for interventional clinical studies to ensure adherence to protocols and regulatory guidelines.
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Clinical Research Associate - CRA (All levels)
Thermofisher
Kuala Lumpur, Malaysia
24d
Conduct remote or on-site clinical monitoring and site management to ensure protocol and regulatory compliance, manage documentation, and guarantee subject rights and data reliability.
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Sr. Site Activation Specialist (North America team)
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Iqvia
Remote
24d
Execute country-level Site Activation activities for clinical research studies, ensuring regulatory compliance and document accuracy for investigative sites.
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Clinical Research Associate - Fresher
↗
Technobridge Systems Pvt Ltd
MH, IN
$180k–$264k
24d
Assist in the design, setup, and monitoring of clinical trials by conducting site visits and ensuring compliance with protocols and GCP.
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Clinical Research Associate
Lemonade
Remote
24d
Coordinate and monitor clinical trials for breast cancer diagnosis, treatment, and care, ensuring site compliance and data integrity.
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FSP Sr Clinical Research Associate I
Thermofisher
Remote, Vietnam
25d
Senior Clinical Research Associate responsible for the preparation, initiation, monitoring, and closure of clinical study sites to ensure compliance with ICH-GCP and local regulations.
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Sr. Clinical Research Assistant - Phoenix, Arizona or Salt Lake City, Utah or Denver, Colorado area - home base required
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US
25d
Senior Clinical Research Associate supporting the execution of clinical studies for a medical device therapy treating dry age-related macular degeneration (dAMD).
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FSP Clinical Research Associate II
Thermofisher
Remote, Vietnam
25d
Monitor clinical study conduct at allocated sites to ensure compliance with ICH-GCP, AZ procedures, and local regulations, acting as the main contact for study sites.
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Sr. Clinical Research Assistant - In or around Chicago, Illinois or Detroit, Michigan area
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US
25d
Senior Clinical Research Associate supporting the execution of clinical studies for a medical device therapy treating dry age-related macular degeneration (dAMD).
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Sr CRA I/II - FSP - Germany
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Thermo Fisher Scientific
Home Office, DE
25d
Senior Clinical Research Associate monitoring investigator sites for cell therapy clinical trials to ensure compliance with ICH GCP and protocol requirements.
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Clinical Research Associate
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Novartis
NSW, AU
25d
Ensure sustainable trial execution at clinical sites for Phase I-IV GDD trials through on-site and remote monitoring activities.
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Clinical Research Associate II
Iqvia
Auckland, North Island
25d
Ensure study sites are compliant and thriving, driving study progress from selection to close-out while managing recruitment and documentation.
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Clinical Research Associate
Precision Medicine Group
Remote, Germany
25d
Monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocol, SOPs, and regulations.
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Clinical Research Associate I (FSP)
Thermo-Fisher-Scientific
Sydney, New South Wales
25d
Conduct remote and on-site clinical monitoring and site management to ensure protocol and regulatory compliance for clinical trials.
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Clinical Research Associate II
Iqvia
Auckland, North Island
25d
Ensure study sites are compliant and thriving to drive advancements in healthcare through clinical research.
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Senior Clinical Research Associate
ICON Clinical Research
Italia
25d
Oversee and manage clinical trial activities to ensure adherence to protocols, regulatory requirements, and GCP standards.
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Clinical Research Associate
BeiGene
Milano, Provincia di Milano
$45k–$45k
26d
Executes clinical monitoring activities at trial sites to ensure data quality and regulatory compliance for oncology/hematology 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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