🔥 3 hours ago
Clinical Trials Associate supporting clinical documentation and project tracking for Worldwide Clinical Trials, a global CRO. Maintaining trial files, project portals, system access, and quality-controlled records.
🔥 5 hours ago
Clinical Research Associate monitoring and managing New Zealand clinical trials for global CRO Emerald Clinical Trials. Supporting site selection, regulatory submissions, compliance, investigator training, and recruitment across renal, cardiometabolic, and oncology studies.
🔥 5 hours ago
Clinical Research Associate monitoring Australian clinical trials for Emerald Clinical Trials, a global clinical research company. Managing sites, regulatory submissions, trial documentation, investigational products, and recruitment support.
🔥 6 hours ago
Clinical Research Associate monitoring clinical trial sites for GT Medical Technologies, a medical technology company. Supporting protocol compliance, data quality, site management, and study milestones across a travel-heavy territory.
🔥 11 hours ago
Clinical Research Associate conducting site monitoring and data-integrity oversight for Syneos Health’s integrated biopharmaceutical services. Supporting clinical and real-world late-phase studies across Ireland through site management, documentation, and compliance activities.
🔥 18 hours ago
Clinical Research Associate advancing AbbVie’s innovative medicines through clinical trial site monitoring in Seoul. Ensuring patient safety, data integrity, regulatory compliance, and study performance.
🗣️🇰🇷 Korean Required
🔥 18 hours ago
Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organization. Ensuring protocol compliance, data integrity, patient safety, and high-quality study documentation.
🔥 22 hours ago
Clinical Research Associate monitoring vaccine trials for ICON, a global clinical research organisation. Coordinating study setup, documentation, compliance, and investigator relationships.
🔥 22 hours ago
Clinical Research Associate monitoring multi-center clinical trials for CIBMTR CRO Services. Supporting site management, compliance, data review, and study execution.
🔥 23 hours ago
Clinical Operations Assistant supporting site coordination and clinical trial administration at Parexel, a global clinical research organization. Managing documents, payments, supplies, and Case Report Forms for Latin American project teams.
🌐 Brazil, Mexico, +1 more countries – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🏥 Clinical Operations
🕒 Yesterday
Clinical trial coordinator supporting site activation, regulatory documentation, and feasibility activities for Thermo Fisher Scientific. Maintaining trial systems, site files, metrics, and investigator communications for clinical research projects.
🇨🇴 Colombia – Remote
⏰ Full Time
🟢 Junior
🟡 Mid-level
✨ Clinical Trial Coordinator
🚫👨🎓 No degree required
🕒 Yesterday
Clinical Research Associate II monitoring oncology clinical trials for BeOne, a global cancer therapeutics company. Managing sites, data quality, safety, compliance, training, and study milestones across Brazil.
🕒 Yesterday
Clinical Trial Associate coordinating clinical trials for ICON, a global clinical research organization. Maintaining trial documentation, supporting regulatory materials, and tracking study milestones.
🕒 Yesterday
Clinical Research Associate II monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organization. Ensuring protocol compliance, data integrity, and patient safety across study sites.
🕒 Yesterday
Clinical Research Associate conducting U.S. clinical trial monitoring for Emerald Clinical Trials. Supporting site activation, compliance, recruitment, data integrity, and investigator relationships.
🕒 Yesterday
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.
🕒 4 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.
🕒 4 days ago
Clinical Review Coordinator conducting Medicare case reviews for Commence’s healthcare data solutions. Supporting physician reviewers, beneficiaries, and QIO healthcare improvement initiatives.
🕒 4 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.
🇵🇱 Poland – Remote
💵 zł220k - zł240k / year
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🕒 4 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.
🇵🇱 Poland – Remote
💵 zł220k - zł240k / year
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
+169 More Clinical Trial Assistant Jobs Available!

The average salary for remote clinical trial assistants is $58,167 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 |
|---|---|---|
🟢 Junior Clinical Trial Assistant (1-2 yrs) | 1 | $39,000 |
🟡 Mid-level Clinical Trial Assistant (2-4 yrs) | 4 | $77,500 |
🟠 Senior Clinical Trial Assistant (5-9 yrs) | 1 | $0 |
We analyzed 5 job listings in the last year and found it takes about 43 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 organizational skills, attention to detail, knowledge of clinical trial processes, proficiency in data entry and management, and familiarity with regulatory requirements. Good communication and teamwork skills are also important for remote collaboration.
Typically, a bachelor's degree in life sciences, nursing, or a related field is required. Relevant certifications in clinical research, such as ACRP or SOCRA, can be advantageous. Experience in clinical trials or research may also be beneficial.
Responsibilities include assisting with study documentation, managing trial databases, coordinating communications between stakeholders, monitoring study progress, and ensuring compliance with protocols and regulations. You'll also help prepare reports and maintain study files.
Benefits include flexible work hours, the opportunity to work from any location, reduced commuting costs, and improved work-life balance. Remote work allows for collaboration with diverse teams and access to a broader range of clinical projects.
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