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🔥 8 hours ago
Job not on LinkedIn
Clinical Research Associate II at Thermo Fisher Scientific managing clinical monitoring and site management processes. Ensures compliance with protocols and develops collaborative relationships with investigational sites.
🔥 10 hours ago
Clinical Research Associate designing and analyzing clinical trials at ICON. Collaborating with investigators and ensuring protocol compliance and data integrity throughout the trial process.
🔥 13 hours ago
Clinical Research Associate I/II managing trial conduct and site relationships in Chengdu, China. Ensuring compliance with study protocol and assisting in site management tasks.
🔥 21 hours ago
Job not on LinkedIn
Senior Clinical Research Associate managing clinical trials at investigational sites for Novartis. Ensuring compliance with regulations and high-quality data delivery during study execution.
⚜️ Louisiana, Texas – Remote
💵 $108.5k - $201.5k / year
💰 Debt Financing on 2005-12
⏰ Full Time
🟠 Senior
🔬 Research Analyst
🗣️🇨🇿 Czech Required
🗣️🇸🇰 Slovak Required
🕒 Yesterday
Clinical Research Associate impacting patient lives in diverse therapeutic areas such as Oncology and Hematology at a global clinical research organization.
🕒 Yesterday
Clinical Trials Associate providing administrative and project tracking support for clinical trial teams. Responsibilities include maintaining documentation, coordinating system access, and supporting project related information.
🕒 Yesterday
Clinical Trial Associate at ICON overseeing and supporting clinical trials execution with compliance and efficiency focus. Collaborating with teams to ensure high standards and address trial challenges.
🕒 Yesterday
Job not on LinkedIn
Clinical Review Coordinator conducting case reviews and quality assurance activities in healthcare at Commence. Requires RN or LPN license, located in Las Vegas, NV for remote work.
🕒 Yesterday
Clinical Research Nurse providing high-quality nursing care directly in patients’ homes while supporting important research studies. Requires high level of independence and commitment to patient safety.
🕒 Yesterday
Job not on LinkedIn
Senior Research Coordinator at SEIU leading research teams for union campaigns and programs. Responsible for recruitment, training, and strategic support for effective labor initiatives.
🕒 Yesterday
Senior Clinical Research Associate at ICON overseeing clinical trial activities for adherence to protocols and regulatory standards. Expert in monitoring practices and site management with excellent stakeholder collaboration.
🕒 Yesterday
Clinical Research Associate responsible for designing and analyzing clinical trials at ICON. Collaborating with site staff to ensure protocol compliance and data integrity during the research process.
🕒 Yesterday
Freelance Regional Clinical Trial Coordinator at Rho, a global CRO, handling clinical trial documentation and stakeholder communication across Europe.
🕒 Yesterday
Job not on LinkedIn
Clinical Trial Associate managing multiple tasks in Rater Training Program for clinical trials at Cogstate. Ensuring successful communication between various stakeholders and effective project execution.
🕒 Yesterday
Job not on LinkedIn
Senior Clinical Research Associate managing clinical trials for diagnostics and medical devices at Danaher. Overseeing protocol execution and ensuring compliance with regulatory standards during trial phases.
🇺🇸 United States – Remote
💵 $103k - $130k / year
⏰ Full Time
🟠 Senior
🔬 Research Analyst
🦅 H1B Visa Sponsor
🕒 Yesterday
Job not on LinkedIn
Clinical Trial Assistant facilitating clinical trial activities for Iovance Biotherapeutics. Providing administrative support and managing study materials within clinical operations.
🕒 2 days ago
Clinical Research Associate monitoring clinical studies and ensuring compliance. Engaging with investigative sites and managing study setup activities.
🇹🇷 Turkey – Remote
💰 $75M Private Equity Round on 2015-12
⏰ Full Time
🟢 Junior
🟡 Mid-level
🔬 Research Analyst
🗣️🇹🇷 Turkish Required
🕒 2 days ago
Clinical Research Associate I/II managing clinical studies for Precision Medicine Group. Ensuring compliance with protocols and regulations while providing support at investigative sites.
🗣️🇹🇷 Turkish Required
🕒 2 days ago
Clinical Review Specialist reviewing admissions appropriateness for Banyan Treatment Centers. Focusing on quality patient care, clinical judgment, and collaboration with multidisciplinary teams.
🐊 Florida – Remote
💵 $25 / hour
💰 Series unknown on 2023-07
⏱ Part Time
🟡 Mid-level
🟠 Senior
🔍🏥 Medical Reviewer
🕒 2 days ago
Clinical Research Associate coordinating and monitoring clinical studies in Germany, ensuring compliance with ICH and GCP guidelines. Managing training, data documentation, and issue escalation for study sponsors.
🗣️🇩🇪 German Required
+218 More Clinical Research Coordinator Jobs Available!
The average salary for remote clinical research coordinators is $71,686 per year. This is based on data from 28 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 Research Coordinator (1-2 yrs) | 21 | $68,694 |
🟡 Mid-level Clinical Research Coordinator (2-4 yrs) | 6 | $94,108 |
🟠 Senior Clinical Research Coordinator (5-9 yrs) | 1 | $0 |
We analyzed 22 job listings in the last year and found it takes about 26 days for employers to close a job opening.
We reviewed 28 job postings and found the top 10 skills employers are asking for most often are:
You need strong organizational and communication skills, attention to detail, knowledge of Good Clinical Practice (GCP), and proficiency in data management software. Familiarity with clinical trial processes and regulations is also crucial.
Typically, a degree in life sciences, nursing, or a related field is required. Certification in clinical research (e.g., ACRP or SoCRA) can enhance your qualifications, along with relevant experience in clinical trials.
Responsibilities include coordinating clinical trials, managing study documents, ensuring compliance with protocols and regulations, conducting site visits, and acting as a liaison between study sponsors and site staff.
Benefits include flexible work arrangements, reduced commuting time, a better work-life balance, and the opportunity to collaborate with diverse teams globally. Remote roles can also provide access to a wider range of job opportunities.
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