Clinical Research Professional
6 days ago
About the Role
We are seeking a highly motivated and organized Clinical Research Associate (CRA) to join our team at Parexel International. As a CRA, you will play a key role in the success of our clinical trials by ensuring that sites are properly trained, compliant, and equipped to conduct studies efficiently.
Your Key Responsibilities
- Site Start-up: Establish relationships with investigators and site staff, conduct feasibility and pre-qualification activities, and ensure timely execution of site agreements and confidentiality agreements.
- Qualification Visits: Conduct remote qualification visits, generate visit/contact reports, and identify site issues for resolution.
- Maintenance: Act as a direct point of contact with assigned sites, assess overall integrity of study implementation, and perform problem-solving to address site issues.
- Reporting: Generate visit/contact 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: Problem-solving skills, ability to work independently, sound presentation skills, client-focused approach, and strong computer skills.
About Us
Parexel International is a leading biopharmaceutical services company providing drug development solutions for clients worldwide. We are committed to delivering high-quality results and exceptional service to our clients.
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