CRA in Clinical Trials
6 days ago
Clinical Research Associate Job Summary
We are seeking an experienced Clinical Research Associate (CRA) to join our team at Parexel International. The successful candidate will be responsible for managing clinical trials from start-up to close-out, ensuring that sites are properly trained and compliant.
Main Responsibilities
- Site Monitoring: Conduct on-site visits, evaluate site compliance, and implement corrective actions.
- Study Management: Manage study timelines, develop strategies for patient recruitment and retention, and ensure timely completion of project goals.
- Reporting: Generate regular progress reports, update trial management systems, and submit relevant documents to the Trial Master File.
Requirements
- Education: Degree-level education in a biological science, pharmacy, or other health-related discipline is preferred.
- Experience: Previous relevant work experience is preferred.
- Skills: Excellent problem-solving skills, ability to work independently, and strong communication skills.
About Parexel
Parexel is a leading global contract research organization (CRO) dedicated to supporting the development of innovative new medicines and therapies.
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