🔥 5 hours ago
Senior Clinical Research Associate at Novartis overseeing clinical trials and site relationships across the US. Ensuring compliance and driving high-quality data delivery in clinical research.
🐊 Florida – Remote
💵 $108.5k - $201.5k / year
💰 Debt Financing on 2005-12
⏰ Full Time
🟠 Senior
🔬 Research Analyst
🗣️🇪🇸 Spanish Required
🔥 8 hours ago
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.
🔥 8 hours ago
Senior Clinical Research Associate overseeing clinical trial management and site relationships at Novartis. Ensuring compliance and high-quality data delivery for patient-centric research studies.
⚜️ Louisiana, Texas – Remote
💵 $108.5k - $201.5k / year
⏰ Full Time
🟠 Senior
🔬 Research Analyst
🦅 H1B Visa Sponsor
🗣️🇨🇿 Czech Required
🗣️🇸🇰 Slovak Required
🔥 8 hours ago
Senior Clinical Research Associate managing clinical trials at Novartis. Building site relationships and ensuring compliance with regulatory requirements through remote monitoring and support.
🐊 Florida – Remote
💵 $108.5k - $201.5k / year
⏰ Full Time
🟠 Senior
🔬 Research Analyst
🦅 H1B Visa Sponsor
🗣️🇪🇸 Spanish Required
🔥 10 hours ago
Senior Clinical Research Associate in complex cardiac medical device studies in Canada. Supporting A-fib clinical studies requiring expertise in electrophysiology and devices.
🗣️🇫🇷 French Required
🔥 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.
🔥 11 hours ago
Senior Clinical Research Associate managing clinical studies and ensuring GCP compliance while coordinating site activities and supporting trial operations.
🔥 11 hours ago
Senior Clinical Research Associate managing quality clinical trial execution for Everest Clinical Research. Interacting with study sponsors, sites, and teams in compliance with regulations.
🇺🇸 United States – Remote
💵 $125k - $145k / year
⏰ Full Time
🟠 Senior
🔬 Research Analyst
🦅 H1B Visa Sponsor
🔥 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
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
Associate Manager of Clinical Monitoring overseeing clinical site management and monitoring activities for Crinetics. Supporting clinical trial operations with a focus on endocrine disorders and risk-based monitoring.
🕒 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
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
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 Research Associate ensuring compliance with ICH-GCP and regulatory requirements. Collaborating with site staff on monitoring, management activities, and patient recruitment throughout the study lifecycle.
🗣️🇩🇪 German Required
🕒 Yesterday
Clinical Trial Assistant facilitating clinical trial activities for Iovance Biotherapeutics. Providing administrative support and managing study materials within clinical operations.
+340 More Clinical Research Associate Jobs Available!
The average salary for remote clinical research associates is $119,319 per year. This is based on data from 1,384 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 |
|---|---|---|
⚪️ Entry-level Clinical Research Associate (0 yrs) | 1 | $0 |
🟢 Junior Clinical Research Associate (1-2 yrs) | 711 | $106,710 |
🟠 Senior Clinical Research Associate (5-9 yrs) | 666 | $132,382 |
🔴 Lead Clinical Research Associate (10+ yrs) | 6 | $183,333 |
We analyzed 1,033 job listings in the last year and found it takes about 34 days for employers to close a job opening.
We reviewed 1,384 job postings and found the top 10 skills employers are asking for most often are:
You need strong analytical skills, attention to detail, knowledge of clinical trial protocols, and understanding of regulatory guidelines. Effective communication, organization, and problem-solving skills are also crucial for remote work.
Typically, a degree in life sciences or a related field is required. Previous experience in clinical research is highly valued, and certifications like CRC or CRA can enhance your qualifications.
Responsibilities include monitoring clinical trials, ensuring compliance with regulatory standards, maintaining study documentation, coordinating with clinical sites, and communicating with stakeholders. You may also be involved in data collection and analysis.
Benefits include flexible working arrangements, reduced commuting time, and the freedom to work from various locations. It also allows for a better work-life balance and opportunities to collaborate with global teams.
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