OR · Remote
$90K - $120K/yr
Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, SOPs, and applicable regulatory guidelines. * Conduct Site Initiation Visits (SIV), Site Monitoring Visits (SMV), and ...
Quick apply
OR · Remote
$90K - $120K/yr
Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, SOPs, and applicable regulatory guidelines. * Conduct Site Initiation Visits (SIV), Site Monitoring Visits (SMV), and ...
OR · Remote
$90K - $120K/yr
Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, SOPs, and applicable regulatory guidelines. * Conduct Site Initiation Visits (SIV), Site Monitoring Visits (SMV), and ...
Quick apply
OR · Remote
$90K - $120K/yr
Monitor clinical trial sites to ensure compliance with study protocols, ICH-GCP, SOPs, and applicable regulatory guidelines. * Conduct Site Initiation Visits (SIV), Site Monitoring Visits (SMV), and ...
$28.82 - $34.93
4% of jobs
$34.93 - $41.04
6% of jobs
$41.04 - $47.16
7% of jobs
$51.74 is the 25th percentile. Wages below this are outliers.
$47.16 - $53.27
9% of jobs
$53.27 - $59.38
15% of jobs
The median wage is $62.08 / hr.
$59.38 - $65.50
18% of jobs
$69.85 is the 75th percentile. Wages above this are outliers.
$65.50 - $71.61
21% of jobs
$71.61 - $77.72
7% of jobs
$77.72 - $83.83
6% of jobs
$83.83 - $89.95
3% of jobs
$89.95 - $96.06
2% of jobs
$28
$62
$96
A Remote Clinical Trial job involves managing or supporting clinical research studies from a remote location rather than on-site at a hospital or research facility. Responsibilities may include data management, patient monitoring, regulatory compliance, and coordinating trial activities. These roles are often held by clinical research associates, coordinators, or data analysts who use digital tools to oversee the trial process. Remote roles help improve accessibility and efficiency while maintaining compliance with regulatory standards.
To thrive in a Remote Clinical Trial position, you need a strong background in clinical research, regulatory compliance, and data management—often supported by a degree in life sciences or health-related fields. Familiarity with electronic data capture (EDC) systems, clinical trial management software (CTMS), and certifications like GCP (Good Clinical Practice) are highly beneficial. Exceptional organizational skills, attention to detail, and proactive communication are essential soft skills for remote collaboration and project management. These abilities ensure accurate trial execution, compliance with protocols, and seamless teamwork across distributed environments.
One of the main challenges in remote clinical trial roles is maintaining effective communication and collaboration with research teams, participants, and stakeholders across various locations. This can be managed by utilizing secure collaboration tools, scheduling regular virtual check-ins, and following clear documentation practices. Remote professionals may also face difficulties in monitoring protocol compliance and data integrity without onsite presence, making strong organizational skills and familiarity with virtual monitoring tools essential. Being proactive and adaptable helps you address issues promptly and ensures study milestones are met. With the right support and resources, remote clinical trial professionals can seamlessly contribute to successful trial outcomes.
$90K - $120K/yr
Full-time
Medical
Re-posted 2 days ago
We are seeking a detail-oriented and motivated Clinical Research Associate (CRA) to oversee and monitor clinical trials while ensuring compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. The ideal candidate will have experience in site monitoring, clinical trial management, and maintaining high-quality clinical data.
Key Responsibilities
Required Qualifications
Preferred Skills
Benefits
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