Job Summary
The Freelance Clinical Research Associate (CRA) plays a critical role in supporting clinical trials and ensuring adherence to study protocols. This position requires monitoring the progress of clinical studies, verifying data accuracy, and ensuring compliance with regulatory standards.
Responsibilities
- Monitor clinical trial sites to ensure compliance with study protocols and regulatory requirements.
- Conduct site visits, including initiation, monitoring, and closeout visits.
- Review and verify source documents against case report forms for data integrity.
- Collaborate with clinical team members to address site issues and facilitate trial progress.
- Assist in the preparation and management of study documentation and reports.
- Provide training and support to site staff regarding study protocols and procedures.
Qualifications
- Bachelor’s degree in Life Sciences or a related field.
- Prior experience in clinical research or related roles, preferably as a CRA.
- Understanding of Good Clinical Practice (GCP) and regulatory guidelines.
- Excellent organizational skills and attention to detail.
- Strong communication skills, both written and verbal.
- Ability to work independently and manage multiple tasks effectively.
