Is on LinkedIn?
🔥 10 minutes ago
Clinical Trial Associate coordinating clinical trials for ICON, a global clinical research organization. Maintaining trial documentation, supporting regulatory materials, and tracking study milestones.
🔥 10 minutes 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
🔥 35 minutes 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
🔥 1 hour 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 Trial Specialist II supporting U.S. pharmaceutical drug development and clinical research. Managing investigative sites, regulatory documents, remote monitoring, TMF readiness, and payments.
🕒 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.
🕒 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.
🕒 2 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.
🕒 2 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
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
Senior Clinical Associate overseeing clinical trials for ICON, a global clinical research organisation. Coordinating sites, ensuring regulatory compliance, maintaining data integrity, and mitigating study risks.
Job not on LinkedIn
🕒 3 days ago
Job not on LinkedIn
Monitor de Pesquisa Clínica Pleno conduzindo estudos farmacêuticos na Synvia. Liderando monitoramento de centros, auditorias, mitigação de riscos e qualidade de dados clínicos.
🗣️🇧🇷🇵🇹 Portuguese Required
🕒 3 days ago
Senior Clinical Research Associate supporting ICON’s Phase I oncology clinical trials. Managing investigative sites, monitoring data integrity, and ensuring subject safety and inspection readiness.
🕒 4 days ago
Clinical Data Associate supporting clinical data management for Rho, a contract research organization. Building and validating EDC databases, programming SAS listings, and identifying data discrepancies.
Job not on LinkedIn
🕒 4 days ago
Job not on LinkedIn
Senior Clinical Research Associate monitoring clinical trials for Thermo Fisher Scientific’s life sciences services. Ensuring regulatory compliance, data integrity, site performance, and audit readiness across Australia.
🕒 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.
🕒 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.
🌽 Illinois, Kentucky, +3 more states – Remote
💵 $110.5k - $138.2k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
✨ Clinical Liaison
Job not on LinkedIn
🕒 4 days ago
Job not on LinkedIn
Senior Clinical Trial Coordinator supporting Thermo Fisher Scientific’s clinical research services remotely in Argentina. Detailed responsibilities and qualifications are not provided in the posting.
+268 More Clinical Trial Associate Jobs Available!
The average salary for remote clinical trial associates is $88,213 per year. This is based on data from 26 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 Associate (1-2 yrs) | 21 | $75,883 |
🟠 Senior Clinical Trial Associate (5-9 yrs) | 5 | $140,000 |
We analyzed 17 job listings in the last year and found it takes about 11 days for employers to close a job opening.
We reviewed 26 job postings and found the top 10 skills employers are asking for most often are:
You need strong organizational skills, attention to detail, analytical thinking, and excellent communication abilities. Proficiency in clinical trial software and knowledge of regulatory guidelines is also important.
Typically, a degree in life sciences, nursing, or a related field is required. Experience in clinical trials or a certification like Clinical Research Associate (CRA) can be advantageous.
Responsibilities include managing trial documentation, ensuring compliance with regulatory requirements, coordinating with study sites, monitoring data quality, and assisting in the preparation of reports and submissions.
Benefits include flexible working conditions, the ability to balance personal and professional life, access to diverse clinical projects, and potential for growth within the industry without the need for daily commuting.
We scan the internet everyday and find jobs not posted on LinkedIn or other job boards.
We find jobs as soon as they're posted, so you can apply before everyone else.
Most members hear back within the first week
We find jobs other job boards miss.
