đ„ 28 minutes ago
Clinical Research Associate monitoring clinical trials for Emerald Clinical Trials, a global clinical research partner. Conducting site visits, validating data, and supporting investigator sites across the trial lifecycle.
đ„ 6 hours ago
Clinical Operations Coordinator supporting CVS Healthâs clinical data and request-processing operations. Managing data entry, validation, database maintenance, reporting, and administrative queries remotely.
đ 2 days ago
Study Coordinator supporting remote clinical trials for UBC, a pharmaceutical support services leader. Managing participants, clinical data, investigational drugs, compliance, and study coordination.
đ 2 days ago
Clinical Trial Specialist II supporting U.S. pharmaceutical drug development and clinical research. Managing investigative sites, regulatory documents, remote monitoring, TMF readiness, and payments.
đ 2 days ago
Clinical trial lead overseeing operational delivery of pharmaceutical and device studies for Precision Medicine Group. Managing sites, monitoring, regulatory submissions, vendors, data quality, and clinical teams.
đșđž United States â Remote
đ” $110.7k - $200.9k / year
đ° $75M Private Equity Round on 2015-12
â° Full Time
đ Senior
đ§Ș Clinical Research
đ 2 days ago
Clinical Project Manager leading clinical trials for Clarioâs clinical evidence solutions. Managing study plans, teams, financial tracking, SOP compliance, stakeholder communication, and project closeout.
đšđ· Costa Rica â Remote
đ° Private Equity Round on 2019-10
â° Full Time
đą Junior
đ„ Clinical Operations
đ 2 days ago
Clinical Research Associate monitoring oncology and HemeONC clinical trials for ICON, a global clinical research organization. Conducting site visits, ensuring compliance, and supporting patient safety and data quality.
đ 2 days ago
Clinical Review Coordinator conducting Medicare case reviews for Commenceâs healthcare data solutions. Supporting physician reviewers, beneficiaries, and QIO healthcare improvement initiatives.
đ° Nevada â Remote
đ” $60k - $83.2k / year
â° Full Time
đą Junior
đĄ Mid-level
âš Clinical Coordinator
đ 3 days ago
Clinical Research Associate conducting site management and monitoring for oncology studies at Parexel, a global CRO. Supporting a dedicated sponsor with clinical trial delivery from a home-based Poland role.
đ”đ± Poland â Remote
đ” zĆ220k - zĆ240k / year
đ° Venture Round on 1990-01
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ 3 days ago
Clinical Trial Manager leading oncology clinical research projects at ICON, a global healthcare intelligence and clinical research organization. Coordinating teams, budgets, timelines, risks, and stakeholder reporting.
đ 3 days ago
Clinical Trial Manager leading Phase I oncology trials for ICON, a global healthcare intelligence and clinical research organisation. Managing vendors, sites, budgets, timelines, data, and regulatory compliance.
đ 3 days ago
Clinical Project Manager leading complex, compliant clinical trials for biopharmaceutical companies in Australia. Managing sponsors, vendors, budgets, risks, and Trial Master File documentation from start-up through closeout.
đ 4 days ago
Clinical Trial Associate supporting ICON, a global healthcare intelligence and clinical research organisation. Coordinating trial documentation, regulatory compliance, study materials, and milestones.
đ 4 days ago
Clinical Project Manager leading US clinical projects for ICON, a global clinical research organization. Coordinating timelines, budgets, risks, stakeholders, and cross-functional teams.
đ 4 days ago
Clinical Trial Liaison supporting ICON, a global clinical research organisation, through investigator management and enrollment strategy. Advancing clinical trials, site performance, and innovative treatments across eligible US states.
đœ Illinois, Kentucky, +3 more states â Remote
đ” $110.5k - $138.2k / year
â° Full Time
đĄ Mid-level
đ Senior
âš Clinical Liaison
đ 4 days ago
Senior Clinical Trial Coordinator supporting Thermo Fisher Scientificâs clinical research services remotely in Argentina. Detailed responsibilities and qualifications are not provided in the posting.
đ 4 days ago
Clinical Trial Manager overseeing global CRISPR cell-therapy trials at Caribou Biosciences. Managing CROs, vendors, data quality, regulatory compliance, and study execution from start-up through close-out.
đ California â Remote
đ” $160k - $175k / year
đ° $125M Post-IPO Equity on 2023-07
â° Full Time
đĄ Mid-level
đ Senior
đ§Ș Clinical Research
đŠ H1B Visa Sponsor
đ 4 days ago
Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Ensuring protocol compliance, data integrity, patient safety, and high-quality study documentation.
đ 4 days ago
Clinical Trial Liaison supporting investigators, sites, and patient recruitment for ICONâs clinical research trials in France. Translating scientific expertise into local study-enrolment strategies.
đŁïžđ«đ· French Required
đ 4 days ago
Clinical Trial Liaison supporting investigators, sites, and patient recruitment for ICONâs clinical research trials in France. Translating scientific expertise into local study-enrolment strategies.
đŁïžđ«đ· French Required
+152 More Clinical Trial Coordinator Jobs Available!

The average salary for remote clinical trial coordinators is $33,140 per year. This is based on data from 43 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 Trial Coordinator (1-2 yrs) | 15 | $95,000 |
đĄ Mid-level Clinical Trial Coordinator (2-4 yrs) | 25 | $0 |
đ Senior Clinical Trial Coordinator (5-9 yrs) | 2 | $0 |
đŽ Lead Clinical Trial Coordinator (10+ yrs) | 1 | $0 |
We analyzed 31 job listings in the last year and found it takes about 14 days for employers to close a job opening.
We reviewed 43 job postings and found the top 10 skills employers are asking for most often are:
You need strong organizational and project management skills, attention to detail, knowledge of clinical trial regulations, and proficiency in data management software. Effective communication and problem-solving skills are also critical for remote coordination.
Typically, you need a degree in life sciences, nursing, or a related field, along with experience in clinical research. Certifications like CCRP or CCRC can enhance your qualifications.
Responsibilities include planning and overseeing clinical trials, managing trial documentation, ensuring compliance with regulatory requirements, coordinating with investigators and study participants, and monitoring trial progress and data integrity.
Benefits include flexibility in work hours and location, reduced commuting, opportunities to work with diverse teams and projects, and a chance to contribute to important medical research advancements.
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