Clinical Research Associate to execute clinical monitoring activities at clinical trial sites, monitor clinical trials, and collaborate with Regional Clinical Operations Manager to ensure study timelines are adhered to and required quality standards are maintained.
Requirements
- BS in a relevant scientific discipline
- Minimum of 2 years of monitoring experience
- Experience in oncology global trials preferred
- Excellent communication and interpersonal skills
- Excellent organizational skills and ability to prioritize and multi-task
- Fluent in English & German (writing and speaking)
- Computer Skills: Efficient in Microsoft Word, Excel, MS Project, MS PowerPoint and Outlook
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
