Location: Remote
Job Type: Contract
About the Role:
As a Clinical Research Associate, you’ll play a crucial role in monitoring clinical trial sites, ensuring compliance with Good Clinical Practice (GCP) guidelines, and maintaining high-quality data integrity. You’ll work closely with investigators, site staff, and sponsors to make sure studies are conducted efficiently and ethically.
What You’ll Do:
- Monitor clinical trial sites to ensure protocol adherence and regulatory compliance
- Conduct site visits (remote and on-site) to oversee data collection and patient safety
- Train and support site staff on study procedures and regulatory requirements
- Verify Case Report Forms (CRFs) against source documents for accuracy
- Identify and address any issues that could impact study quality or timelines
- Ensure proper documentation and reporting of adverse events
Collaborate with cross-functional teams, including project managers and regulatory affairs
What We’re Looking For:
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or a related field
- 1+ years of experience in clinical research (CRA, CTA, or study coordinator roles preferred)
- Strong knowledge of ICH-GCP, FDA, and other regulatory guidelines
- Excellent attention to detail and problem-solving skills
- Willingness to travel [mention % of travel required]
- Strong communication and teamwork skills
Why our Client?
- Work on ground-breaking clinical trials that make a real impact on patient’s lives
- Career growth opportunities in a fast-paced, innovative environment
- Competitive salary + benefits (healthcare, PTO, 401k, etc.)
- Apply Now – [email protected]