Clinical Research Associate
Virtual Vocations Inc
To support clinical trial initiatives, the freelance Clinical Research Associate (0.4 FTE) will conduct remote and on-site monitoring, ensuring compliance with regulatory requirements and data integrity while working fully remotely. Key Responsibilities: Monitor clinical trials to ensure subject safety, data integrity, and compliance with GCP and ICH guidelines Verify informed consent procedures and protocol adherence at study sites Prepare monitoring visit reports and maintain accurate site documentation in project systems Required Qualifications: Bachelor's Degree in Life Sciences, Nursing, or a related field Minimum 1 year of relevant clinical research experience or academic background in clinical trials Understanding of Good Clinical Practice (GCP) and ICH guidelines Fluency in English with strong written and verbal communication skills Excellent organizational skills and ability to work independently in a matrix team environment
Vacancy posted 5 days ago
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