Clinical Research Associate
4 weeks ago
Role Overview
As a Clinical Research Associate - Sponsor Dedicated, you will be responsible for performing site monitoring visits, working with sites to adapt and drive subject recruitment plans, and administering protocol and related study training.
Key Responsibilities
- Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
- Work with sites to adapt and drive subject recruitment plans
- Administer protocol and related study training to assigned sites
- Evaluate the quality and integrity of study site practices
- Manage the progress of assigned studies by tracking regulatory submissions and approvals
- Ensure copies/originals of site documents are available for filing in the Trial Master File
Requirements
- Life science degree education
- Independent on-site monitoring experience
- Experience handling multiple protocols and sites across various drug indications
- Flexibility and ability to travel
- Strong communication, written, and presentation skills
About IQVIA
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
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