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đ 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.
đ 2 days ago
Clinical Research Associate monitoring sites and protocols for Merck, a global healthcare company developing medicines, vaccines, and animal health products. Managing compliance, documentation, recruitment, and site performance across U.S. territories.
đ California, Colorado, +5 more states â Remote
đ” $96.2k - $151.4k / year
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đŠ H1B Visa Sponsor
đ 2 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.
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
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.
đ 2 days ago
Senior Clinical Research Associate supporting ICONâs oncology clinical trials in Philadelphia or Baltimore. Managing investigative-site monitoring, compliance, data integrity, and inspection readiness.
Job not on LinkedIn
đ 2 days ago
Job not on LinkedIn
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 2 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 Research Associate advancing AbbVieâs innovative medicines through clinical-trial site monitoring. Supporting investigator sites, recruitment, compliance, data integrity, and patient safety across the US.
đ California â Remote
đ” $75k - $142.5k / year
â° Full Time
đą Junior
đĄ Mid-level
đ§Ș Clinical Research
đ«đšâđ No degree required
đŠ H1B Visa Sponsor
Job not on LinkedIn
đ 3 days ago
Job not on LinkedIn
Monitor de Pesquisa ClĂnica Pleno conduzindo estudos farmacĂȘuticos na Synvia. Liderando monitoramento de centros, auditorias, mitigação de riscos e qualidade de dados clĂnicos.
đŁïžđ§đ·đ”đč Portuguese Required
Job not on LinkedIn
đ 3 days ago
Job not on LinkedIn
Clinician-to-CRA conducting risk-based monitoring and site management for Thermo Fisherâs global clinical research services. Ensuring protocol compliance, data integrity, audit readiness, and trial documentation.
đ 3 days ago
Senior Clinical Research Associate supporting ICONâs Phase I oncology clinical trials. Managing investigative sites, monitoring data integrity, and ensuring subject safety and inspection readiness.
đ 3 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
đ 3 days ago
Job not on LinkedIn
Senior Clinical Research Associate monitoring clinical trials for Thermo Fisher Scientificâs life sciences services. Ensuring regulatory compliance, data integrity, site performance, and audit readiness across Australia.
đ 3 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
Senior Clinical Research Associate overseeing clinical trial monitoring for ICON, a global healthcare intelligence and clinical research organisation. Managing sites, compliance, data integrity, and trial execution across the US.
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
Lead CRA managing monitoring and site-management services for Alimentiv, a clinical research services company. Overseeing site activation, recruitment, data quality, regulatory documentation, and CRA mentoring across clinical studies.
đŁïžđ«đ· French Required
Job not on LinkedIn
đ 4 days ago
Job not on LinkedIn
Clinical Research Associate monitoring clinical trials for Thermo Fisher Scientific, a global life-science services company. Ensuring site compliance, data integrity, documentation, and audit readiness through remote and on-site visits.
Job not on LinkedIn
đ 4 days ago
Job not on LinkedIn
Assistant Clinical Research Associate supporting remote site management and monitoring for Thermo Fisher Scientificâs clinical research programs in Greece. Coordinating documentation, systems, vendors, payments, and trial reconciliations.
+251 More Clinical Research Assistant Jobs Available!
The average salary for remote clinical research assistants is $24,585 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 |
|---|---|---|
đą Junior Clinical Research Assistant (1-2 yrs) | 3 | $49,171 |
đĄ Mid-level Clinical Research Assistant (2-4 yrs) | 3 | $0 |
We analyzed 4 job listings in the last year and found it takes about 22 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 analytical skills, attention to detail, excellent communication abilities, and proficiency in data management software. Knowledge of clinical trial processes and regulations is also important.
Typically, a degree in life sciences, nursing, or a related field is required. Relevant certifications in clinical research can also enhance your qualifications. Experience in medical or research settings is beneficial.
Responsibilities include assisting with study protocols, collecting and analyzing data, maintaining study documentation, ensuring regulatory compliance, and collaborating with study teams and participants.
Benefits of working as a remote Clinical Research Assistant include flexible work arrangements, reduced commuting, the ability to manage your own schedule, and the opportunity to work with diverse teams across different locations.
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.
