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🔥 1 hour ago
Senior Clinical Research Associate conducting onsite monitoring for PSI, a global medical research company. Managing oncology and clinical trial sites, timelines, data quality, and regulatory submissions.
🔥 1 hour ago
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.
🔥 2 hours ago
Senior Clinical Research Associate conducting Phase II/III trial monitoring for a global medical research company. Managing sites, regulatory submissions, audits, and study-team communications in Canada.
🔥 2 hours ago
Senior Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Ensuring protocol compliance, site performance, data integrity, and trial execution.
🔥 2 hours ago
Senior CRA monitoring clinical trials for ICON, a global healthcare intelligence organisation delivering medicines and treatments faster. Overseeing sites, compliance, data integrity, and trial execution across the West Coast.
Job not on LinkedIn
🔥 4 hours ago
Job not on LinkedIn
Clinical Research Associate monitoring and managing clinical trial sites in New Zealand for Emerald Clinical Trials, a global clinical research company. Supporting regulatory submissions, site start-up, compliance, documentation, and recruitment across renal, cardiometabolic, and oncology studies.
🔥 4 hours ago
Clinical Trial Associate coordinating clinical trials for ICON, a global clinical research organization. Maintaining trial documentation, supporting regulatory materials, and tracking study milestones.
🔥 4 hours ago
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.
Job not on LinkedIn
🔥 5 hours ago
Job not on LinkedIn
Clinical Research Associate conducting U.S. clinical trial monitoring for Emerald Clinical Trials. Supporting site activation, compliance, recruitment, data integrity, and investigator relationships.
Job not on LinkedIn
🔥 6 hours ago
Job not on LinkedIn
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.
🕒 2 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 delivery.
🕒 3 days ago
In-house Clinical Research Associate supporting site management and data-quality activities for Worldwide Clinical Trials, a global contract research organization. Coordinating clinical-study documentation, monitoring support, queries, recruitment, and site communications.
🕒 3 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.
🕒 3 days ago
Remote Senior Clinical Research Associate conducting oncology site monitoring for ICON, a global clinical research organisation. Managing compliance, patient safety, data quality, and site relationships across Ohio and the northeast region.
🕒 3 days ago
Senior Clinical Research Associate supporting ICON’s oncology clinical trials in Philadelphia or Baltimore. Managing investigative-site monitoring, compliance, data integrity, and inspection readiness.
Job not on LinkedIn
🕒 3 days ago
Job not on LinkedIn
Clinical Review Coordinator conducting Medicare case reviews for Commence’s healthcare data solutions. Supporting physician reviewers, beneficiaries, and QIO healthcare improvement initiatives.
🕒 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.
🇵🇱 Poland – Remote
💵 zł220k - zł240k / year
💰 Venture Round on 1990-01
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🕒 3 days ago
Research Data Coordinator managing clinical and translational datasets at Bristol Myers Squibb. Supporting FAIR, AI-ready data and vendor data transfers across drug development.
🇺🇸 United States – Remote
💵 $128.9k - $156.2k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
✨ Research Coordinator
🦅 H1B Visa Sponsor
🕒 3 days ago
Clinical Research Associate advancing AbbVie’s innovative medicines through clinical-trial site monitoring. Supporting investigator sites, recruitment, compliance, data integrity, and patient safety across the US.
🏄 California – Remote
💵 $75k - $142.5k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🚫👨🎓 No degree required
🦅 H1B Visa Sponsor
🕒 3 days ago
Clinical Research Associate advancing AbbVie’s innovative medicines through clinical-trial site monitoring. Supporting investigator sites, recruitment, compliance, data integrity, and patient safety across the US.
🏄 California – Remote
💵 $75k - $142.5k / year
⏰ Full Time
🟢 Junior
🟡 Mid-level
🧪 Clinical Research
🚫👨🎓 No degree required
🦅 H1B Visa Sponsor
+247 More Research Coordinator Jobs Available!
The average salary for remote research coordinators is $72,174 per year. This is based on data from 40 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 Research Coordinator (1-2 yrs) | 27 | $63,030 |
🟡 Mid-level Research Coordinator (2-4 yrs) | 9 | $85,956 |
🟠 Senior Research Coordinator (5-9 yrs) | 4 | $102,886 |
We analyzed 27 job listings in the last year and found it takes about 29 days for employers to close a job opening.
We reviewed 40 job postings and found the top 10 skills employers are asking for most often are:
You need strong analytical and organizational skills, proficiency in research methodologies, and experience with data analysis tools. Excellent communication and collaboration skills are also vital for working with remote teams and stakeholders.
Typically, a degree in social sciences, public health, or a related field is required. Experience in research project management and a strong understanding of research ethics are important. Certifications in research methods or data analysis can also be advantageous.
Responsibilities include designing and implementing research studies, coordinating with researchers and participants, managing data collection and analysis, ensuring compliance with ethical standards, and reporting findings to stakeholders.
Benefits include flexible work hours, the ability to work from various locations, reduced commuting costs, and a better work-life balance. Remote work also allows for collaboration with diverse teams and access to a wider range of research opportunities.
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