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You are a Clinical Research Associate (CRA), you will be responsible for ensuring the successful conduct of clinical trials from initiation to closeout. You’ll collaborate with investigators, study coordinators, and internal cross-functional teams, including Research and Development, Finance, and Marketing—to ensure compliance with regulatory requirements and Good Clinical Practice (GCP). This role requires attention to detail, strong communication, and the ability to manage multiple projects simultaneously.
Location: Remote and 15% Travel
Salary Range: $35 – $45
How You’ll Make An Impact:
- Conduct Site Initiation, Routine Monitoring, and Close out visits to ensure adherence to protocols, regulatory requirements, and good clinical practice
- Perform source data verification, data collection, and query resolution to ensure accurate study data
- Maintain and manage study documentation including regulatory documents and trial master files
- Work closely with cross-functional teams to ensure timely study execution
- Prepare and submit monitoring visit reports, letters, and other study-related documentation
What You Bring:
- Education: Bachelors Degree
- Work Experience: A minimum of 1-2 year of experience as a CRA or similar role
- Strong understanding of clinical trial processes, regulations, and guidelines
- Excellent communication, organization, and time management skills
- CRA certification is a plus
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