Selected: âš Clinical Research Assistant.
Selected: đ Date Added.
đ„ 2 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„ 2 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„ 2 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„ 3 hours ago
Clinical Trial Coordinator supporting pharmaceutical and biotech sponsors with trial documentation, feasibility, regulatory submissions, and site activation. Maintaining study systems, coordinating sites, and supporting global project teams.
đ·đž Serbia â Remote
â° Full Time
đĄ Mid-level
đ Senior
âš Clinical Trial Coordinator
đ» Ghost score 10%
đ„ 6 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„ 12 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„ 18 hours ago
Clinical Study Operations Associate supporting clinical study startup, site management, and monitoring for Beacon Biosignalsâ at-home EEG platform. Ensuring device deployment, data quality, and regulatory compliance.
đșđž United States â Remote
đ” $65k - $85k / year
â° Full Time
đą Junior
đĄ Mid-level
đ„ Clinical Operations
đ«đšâđ No degree required
đ» Ghost score 14%
đ„ 21 hours ago
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 Yesterday
Remote Clinical Research Associate managing cardiovascular clinical trial sites for Merck & Co. Ensuring ICH/GCP compliance, monitoring sites, and supporting study execution with 65%-75% travel.
đïž New Jersey â Remote
đ” $96.2k - $151.4k / year
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đŠ H1B Visa Sponsor
đ» Ghost score 0%
đ Yesterday
Clinical Trial Associate II supporting clinical trial operations for Ora's ophthalmic drug and device development programs. Managing regulatory documents, trial files, site activities, and study closeout.
đșđž United States â Remote
â° Full Time
đą Junior
đĄ Mid-level
âš Clinical Trial Associate
đŠ H1B Visa Sponsor
đ» Ghost score 10%
đ Yesterday
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 Yesterday
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 Yesterday
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 Yesterday
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 pharmaceutical clinical trials and investigational sites. Ensuring regulatory compliance, data accuracy, documentation, and audit readiness across global research programs.
đźđ± Israel â Remote
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ» Ghost score 10%
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%
đ 2 days ago
Remote Clinical Research Associate monitoring oncology clinical trials for ICONâs sponsor-dedicated research programs. Ensuring compliance, data integrity, patient safety, and quality study documentation.
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%
+335 More Clinical Research Assistant Jobs Available!

The average salary for remote clinical research assistants is $24,585 per year. This is based on data from 6 job openings. Our advanced AI searches the internet for remote job openings and posts them on our website. We use the salary data from these job postings to calculate salary expectations.
Below is a breakdown of salary data by years of experience:
| Experience | Number of roles analyzed | Average Salary |
|---|---|---|
đą Junior Clinical Research Assistant (1-2 yrs) | 3 | $49,171 |
đĄ Mid-level Clinical Research Assistant (2-4 yrs) | 3 | $0 |
We analyzed 4 job listings in the last year and found it takes about 22 days for employers to close a job opening.
We reviewed 6 job postings and found the top 10 skills employers are asking for most often are:
You need strong analytical skills, attention to detail, excellent communication abilities, and proficiency in data management software. Knowledge of clinical trial processes and regulations is also important.
Typically, a degree in life sciences, nursing, or a related field is required. Relevant certifications in clinical research can also enhance your qualifications. Experience in medical or research settings is beneficial.
Responsibilities include assisting with study protocols, collecting and analyzing data, maintaining study documentation, ensuring regulatory compliance, and collaborating with study teams and participants.
Benefits of working as a remote Clinical Research Assistant include flexible work arrangements, reduced commuting, the ability to manage your own schedule, and the opportunity to work with diverse teams across different locations.
We scan the internet everyday and find jobs not posted on LinkedIn or other job boards.
We find jobs minutes after they're posted, so you can apply before everyone else.
Most members hear back within the first week
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