Selected: ⨠Clinical Trial Coordinator.
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Selected: đ Date Added.
đ Yesterday
Clinical Trial Manager overseeing global Phase 3 oncology studies for Summit Therapeutics, a biopharmaceutical company. Managing CROs, sites, clinical data, regulatory compliance, and trial quality.
đ United Kingdom, Ireland â Remote
đľ $67k - $79k / year
â° Full Time
đĄ Mid-level
đ Senior
đ§Ş Clinical Research
đť Ghost score 14%
đ Yesterday
Senior Clinical Trial Manager leading complex global oncology trials for Summit Therapeutics, a biopharmaceutical company. Overseeing CROs, clinical data, quality, regulatory readiness, and study closeout.
đŹđ§ United Kingdom â Remote
đľ ÂŁ71.6k - ÂŁ85k / year
â° Full Time
đ Senior
đ§Ş Clinical Research
đť Ghost score 14%
đ Yesterday
Clinical Research Associate monitoring sponsor-dedicated cardio and obesity clinical trials for ICON Strategic Solutions. Conducting site visits, ensuring protocol compliance, and maintaining clinical data quality.
đ Florida, Texas â Remote
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 10%
đ Yesterday
Clinical Research Associate monitoring sponsor-dedicated cardio and obesity clinical trials for ICON. Conducting site visits, ensuring protocol compliance, and maintaining clinical data integrity.
đ Florida â Remote
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 10%
đ 2 days ago
Clinical Research Associate monitoring clinical trial sites for Syneos Health, a life sciences services company. Ensuring GCP compliance, data integrity, and site performance across Denmark and the Nordics.
đŠđ° Denmark â Remote
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 10%
đŁď¸đŠđ° Danish Required
đ 2 days ago
Senior CRA/Associate CTM supporting GondolaBioâs genetic-disease clinical trials from start-up through closeout. Overseeing sites, CROs, vendors, data, and regulatory compliance remotely.
đşđ¸ United States â Remote
đľ $110k - $120k / year
đ° $300M Venture Round - GondolaBio on 2024-08
â° Full Time
đ Senior
đ§Ş Clinical Research
đť Ghost score 4%
đ 2 days ago
Senior Clinical Trial Manager overseeing global clinical trial planning, vendors, compliance, and execution. Supporting Elevar Therapeuticsâ growing biotech operations, preferably in oncology.
đşđ¸ United States â Remote
đľ $170k - $187k / year
đ° $20M Venture Round - Elevar Therapeutics on 2018-07
â° Full Time
đ Senior
đ§Ş Clinical Research
đť Ghost score 4%
đ 2 days ago
Clinical Research Associate conducting site monitoring and clinical data review for ICONâs sponsor-dedicated trials. Supporting protocol compliance, patient safety, and study documentation.
đŚđş Australia â Remote
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 10%
đ 2 days ago
Clinical Research Associate monitoring investigative sites for Linical, a clinical research organization. Ensuring GCP compliance, participant safety, data integrity, and investigational product accountability.
đşđ¸ United States â Remote
đľ $95k - $135k / year
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 0%
đ 2 days ago
Clinical Research Associate monitoring investigative sites for Linical, a clinical-trial CRO. Ensuring GCP compliance, participant safety, data integrity, and site performance.
đşđ¸ United States â Remote
đľ $95k - $120k / year
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đŤđ¨âđ No degree required
đť Ghost score 0%
đ 2 days ago
Senior Clinical Trial Manager leading global Phase II/III oncology studies at biopharmaceutical company. Overseeing CROs, trial execution, data quality, compliance, and inspection readiness.
đşđ¸ United States â Remote
đľ $158k - $185k / year
â° Full Time
đ Senior
đ§Ş Clinical Research
đť Ghost score 14%
đ 3 days ago
Clinical trial prescreening specialist reviewing EHR charts for a healthcare technology company. Screening patients for specialty-medicine trials and documenting eligibility findings.
đľđ Philippines â Remote
đľ $7 / hour
âł Contract/Temporary
đĄ Mid-level
đ Senior
⨠Clinical Specialist
đť Ghost score 0%
đ 3 days ago
Clinical Research Associate conducting onsite monitoring and study startup activities for PSI, a contract research organization. Managing sites, reviewing clinical data, and supporting regulatory submissions.
đ§đˇ Brazil â Remote
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 10%
đŁď¸đŞđ¸ Spanish Required
đ 3 days ago
Clinical trial manager overseeing clinical monitoring, site management, and risk mitigation for Syneos Healthâs integrated drug-development services. Supporting trial milestones, compliance, data integrity, and study teams.
đ Brazil, Argentina, +3 more countries â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ§Ş Clinical Research
đť Ghost score 10%
đ 3 days ago
Clinical Trial Manager leading end-to-end clinical trials for CareDx, a transplant-focused precision medicine company. Driving study execution, vendor oversight, data quality, and regulatory compliance.
đ California â Remote
đľ $124k - $155k / year
â° Full Time
đĄ Mid-level
đ Senior
đ§Ş Clinical Research
đť Ghost score 0%
đ 3 days ago
Clinical Research Associate monitoring Phase IâIII clinical trials for AbbVie, an innovative medicines company. Ensuring site compliance, data quality, subject safety, and regulatory readiness.
đ¨đŚ Canada â Remote
đľ CAD81k - CAD131k / year
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đŤđ¨âđ No degree required
đť Ghost score 0%
đ 3 days ago
Clinical Research Associate monitoring AbbVieâs Phase IâIII clinical trials and investigative sites. Ensuring protocol compliance, data quality, subject safety, and regulatory readiness across Canada.
đ¨đŚ Canada â Remote
đľ $81k - $131k / year
â° Full Time
đ˘ Junior
đĄ Mid-level
đ§Ş Clinical Research
đŤđ¨âđ No degree required
đť Ghost score 0%
đ 3 days ago
Clinical Research Associate monitoring investigator sites for Parexelâs clinical trials. Ensuring patient safety, GCP compliance, recruitment, and study quality across the Western US.
đşđ¸ United States â Remote
đ° Venture Round on 1990-01
â° Full Time
đ Senior
đ§Ş Clinical Research
đŚ H1B Visa Sponsor
đť Ghost score 10%
đ 3 days ago
Clinical Research Associate conducting site monitoring for oncology and gastroenterology clinical trials. Supporting sponsors and sites through visits, compliance, data verification, and study documentation.
đ¨đŚ Canada â Remote
âł Contract/Temporary
đĄ Mid-level
đ§Ş Clinical Research
đť Ghost score 10%
đ 3 days ago
Clinical Project Coordinator supporting clinical research project administration, documentation, billing, and stakeholder queries at Alimentiv. Home-based role coordinating meetings, training, and clinical study materials.
đ California, New York, +5 more states â Remote
đľ $44k - $73.5k / year
â° Full Time
đ˘ Junior
đˇââď¸ Project Manager
đť Ghost score 2%
+311 More Clinical Trial Coordinator Jobs Available!
The average salary for remote clinical trial coordinators is $73,088 per year. This is based on data from 137 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 Mid-level Clinical Trial Coordinator (2-4 yrs) | 137 | $73,088 |
We analyzed 69 job listings in the last year and found it takes about 26 days for employers to close a job opening.
We reviewed 177 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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