Is on LinkedIn?
🔥 24 minutes ago
Clinical Trials Manager responsible for coordinating clinical studies and monitoring trial sites at Gilead Sciences. Requires 6+ years of experience and a relevant degree.
🇺🇸 United States – Remote
💵 $133.2k - $172.4k / year
💰 $3.5M Post-IPO Debt - Gilead Sciences on 2024-11
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🦅 H1B Visa Sponsor
🔥 3 hours ago
Sr. Clinical Trial Manager overseeing large clinical trials with a focus on biomarker implementation at Syneos Health. Collaborating with local teams and managing regulatory compliance.
🔥 12 hours ago
Clinical Trials Manager coordinating clinical studies and monitoring sites for Gilead. Managing CROs and ensuring effective study practices with a focus on compliance and timelines.
🇺🇸 United States – Remote
💵 $133.2k - $172.4k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🦅 H1B Visa Sponsor
🔥 16 hours ago
Clinical Trial Manager leading complex clinical studies ensuring timelines, costs, and quality metrics are met at Natera. Providing functional expertise to enhance compliance with regulatory standards.
🇺🇸 United States – Remote
💵 $138.6k - $173.3k / year
⏰ Full Time
🟠 Senior
🔴 Lead
🧪 Clinical Research
🦅 H1B Visa Sponsor
🔥 17 hours ago
Job not on LinkedIn
Clinical Study Manager leading and supporting clinical studies in a global medical device company. Focused on orthopedic research and helping surgeons treat their patients better.
🔥 20 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 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
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
Clinical Trial Manager overseeing site management and compliance in cancer immunotherapy trials. Collaborating with diverse teams to drive study execution and operational excellence.
🕒 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
Clinical Trial Manager overseeing site management and monitoring for clinical trials at Syneos Health. Focus on patient safety, compliance, and data integrity in the drug development process.
🗣️🇩🇪 German Required
🕒 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.
🕒 Yesterday
Clinical Trial Leader overseeing clinical trial activities to support biopharmaceutical companies. Providing leadership and management to Clinical Research Associates and ensuring clinical deliverables are met.
🕒 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
Sr. Clinical Research Associate overseeing site activation and management for cardiovascular clinical studies at VahatiCor. Requires significant experience in clinical research and medical device studies.
+166 More Clinical Trial Coordinator Jobs Available!
The average salary for remote clinical trial coordinators is $0 per year. This is based on data from 12 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 Coordinator (1-2 yrs) | 6 | $0 |
🟡 Mid-level Clinical Trial Coordinator (2-4 yrs) | 5 | $0 |
🟠 Senior Clinical Trial Coordinator (5-9 yrs) | 1 | $0 |
We analyzed 4 job listings in the last year and found it takes about 13 days for employers to close a job opening.
We reviewed 12 job postings and found the top 10 skills employers are asking for most often are:
You need strong organizational and project management skills, attention to detail, knowledge of clinical trial regulations, and proficiency in data management software. Effective communication and problem-solving skills are also critical for remote coordination.
Typically, you need a degree in life sciences, nursing, or a related field, along with experience in clinical research. Certifications like CCRP or CCRC can enhance your qualifications.
Responsibilities include planning and overseeing clinical trials, managing trial documentation, ensuring compliance with regulatory requirements, coordinating with investigators and study participants, and monitoring trial progress and data integrity.
Benefits include flexibility in work hours and location, reduced commuting, opportunities to work with diverse teams and projects, and a chance to contribute to important medical research advancements.
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