Selected: âš Medical Research Assistant.
Selected: đ Date Added.
đ„ 1 hour ago
Clinical Research Associate managing site monitoring, compliance, and patient safety for Parexelâs clinical trial services. Supporting investigator sites from activation through close-out across the U.S. West Coast.
â°ïž Colorado â Remote
đ° Venture Round on 1990-01
â° Full Time
đ Senior
đ§Ș Clinical Research
đŠ H1B Visa Sponsor
đ» Ghost score 10%
đ„ 2 hours ago
Senior Clinical Research Associate conducting clinical trial monitoring for Alira Health in Spain. Ensuring site compliance, data integrity, regulatory adherence, and CRA team oversight.
đȘđž Spain â Remote
đ” âŹ45k - âŹ60k / year
đ° $58M Venture Round on 2023-01
â° Full Time
đ Senior
đ§Ș Clinical Research
đ» Ghost score 1%
đ„ 2 hours ago
Senior Clinical Research Associate monitoring oncology clinical trials for Alira Health in Spain. Ensuring GCP compliance, site quality, data integrity, and CRA oversight.
đȘđž Spain â Remote
đ” âŹ45k - âŹ60k / year
đ° $58M Venture Round on 2023-01
â° Full Time
đ Senior
đ§Ș Clinical Research
đ» Ghost score 1%
đ„ 2 hours ago
Senior Clinical Research Associate monitoring clinical trials across Belgium and the Netherlands for Alira Health. Leading CRA oversight, site compliance, data quality, and sponsor coordination.
đ Netherlands, Belgium â Remote
đ” âŹ65k - âŹ80k / year
đ° $58M Venture Round on 2023-01
â° Full Time
đ Senior
đ§Ș Clinical Research
đ» Ghost score 1%
đ„ 2 hours ago
Senior Clinical Research Associate monitoring oncology clinical trials for ICON Strategic Solutions. Managing sites, compliance, data integrity, and CRA guidance in a sponsor-dedicated model.
đïž New Jersey, New York, +3 more states â Remote
đ” $110.5k - $138.2k / year
â° Full Time
đ Senior
đ§Ș Clinical Research
đ» Ghost score 0%
đ„ 2 hours ago
Remote Senior Clinical Research Associate monitoring sponsor-dedicated Phase I oncology trials for ICON. Overseeing sites, compliance, data integrity, and CRA guidance with approximately 60% travel.
đ” Arizona, California, +3 more states â Remote
đ” $110.5k - $138.2k / year
â° Full Time
đ Senior
đ§Ș Clinical Research
đ» Ghost score 0%
đ„ 9 hours ago
Clinical Research Associate monitoring sponsor-dedicated clinical trials for ICON, a global clinical research organization. Ensuring protocol compliance, data integrity, and patient safety.
đŁïžđ©đȘ German Required
đ„ 9 hours ago
Clinical Research Associate monitoring sponsor-dedicated clinical trials for ICON. Ensuring protocol compliance, data integrity, and patient safety in innovative treatment development.
đŁïžđ©đȘ German Required
đ„ 9 hours ago
Clinical Project Assistant supporting clinical research studies at GenesisCare, a cancer-care provider. Coordinating documentation, trial systems, project tracking and team activities remotely.
đŠđș Australia â Remote
đ° Private Equity Round on 2018-10
â° Full Time
đĄ Mid-level
đ Senior
âš Clinical Assistant
đ» Ghost score 12%
đ„ 13 hours ago
Remote Clinical Research Associate II monitoring clinical trials for ICONâs sponsor-dedicated research programs. Ensuring protocol compliance, data integrity, patient safety, and high-quality study data.
đČđŸ Malaysia â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
đ„ 20 hours ago
Clinical Research Coordinator recruiting and managing participants for Science 37âs decentralized clinical trials. Ensuring protocol compliance, accurate data, and regulatory-quality study execution.
đșđž United States â Remote
đ° $200M Post-IPO Equity on 2021-10
âł Contract/Temporary
đĄ Mid-level
đ Senior
đ§Ș Clinical Research
đŠ H1B Visa Sponsor
đ» Ghost score 12%
đ Yesterday
Part-time Research Coordinator supporting archival research and online field experiments at the University of Wisconsin-Madison. Coordinating data collection, IRB documentation, participants, research assistants, and study materials.
đ§ Wisconsin â Remote
đ” $33 / hour
â± Part Time
đĄ Mid-level
đ Senior
âš Research Coordinator
đ» Ghost score 0%
đ Yesterday
Clinical Research Associate II monitoring oncology clinical trials for PSI, a contract research organization. Managing site visits, data integrity, regulatory documents, and investigator communications.
đșđž United States â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
đ 2 days ago
Part-time Clinical Research Coordinator supporting compliant cancer research projects at Cleveland Clinic. Coordinating protocols, regulatory documents, data, audits, and study-team communications.
đ Ohio â Remote
â± Part Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ«đšâđ No degree required
đŠ H1B Visa Sponsor
đ» Ghost score 10%
đ 2 days ago
Clinical Research Associate II advancing AbbVieâs innovative medicines through clinical site monitoring. Managing site engagement, compliance, recruitment, data quality, and patient safety.
đœ Illinois â Remote
đ” $84.5k - $162k / year
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ«đšâđ No degree required
đŠ H1B Visa Sponsor
đ» Ghost score 0%
đ 2 days ago
Senior Clinical Research Associate monitoring clinical sites for Parexel, a clinical development and regulatory solutions provider. Managing site compliance, data quality, and trial documentation.
đ California, Florida, +1 more states â Remote
đ° Venture Round on 1990-01
â° Full Time
đ Senior
đ§Ș Clinical Research
đŠ H1B Visa Sponsor
đ» Ghost score 10%
đ 2 days ago
Clinical Research Associate II conducting on-site and remote monitoring for Ergomedâs complex rare disease and oncology trials. Supporting investigational sites, staff training, and regulatory submissions.
đłđż New Zealand â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 17%
đ 2 days ago
Clinical Research Associate monitoring HemOnc clinical trials for ICON Strategic Solutions. Conducting site visits, ensuring protocol compliance, and maintaining data integrity across California or Colorado.
đ California, Colorado â Remote
đ” $91.3k - $114.2k / year
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 0%
đ 2 days ago
Clinical Research Associate monitoring oncology clinical trials for ICONâs sponsor-dedicated research programs. Ensuring protocol compliance, data integrity, and site performance across assigned regions.
đ California, Texas â Remote
đ” $91.3k - $114.2k / year
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 0%
đ 2 days ago
Remote Clinical Research Associate monitoring oncology clinical trials for ICON Strategic Solutions. Conducting site visits, ensuring ICH-GCP compliance, and maintaining clinical data quality.
đ” Arizona, California, +5 more states â Remote
đ” $91.3k - $114.2k / year
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 0%
+291 More Medical Research Assistant Jobs Available!

Strong analytical and research skills, attention to detail, proficiency in data analysis software, and excellent communication skills. A good understanding of medical terminology and research methodologies is also important.
A degree in life sciences, health sciences, or a related field is typically required. Relevant certifications in research methods or data analysis, along with experience in clinical settings, can be advantageous.
Responsibilities include conducting literature reviews, collecting and analyzing data, assisting in writing research proposals and reports, maintaining research databases, and ensuring compliance with ethical standards and regulations.
Benefits include flexible work hours, the ability to work from various locations, reduced commuting expenses, and improved work-life balance. Remote positions also often provide exposure to diverse research projects and collaboration with professionals across the globe.
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