Clinical Research Associate to pioneer groundbreaking clinical studies, ensuring protocol and regulatory compliance, and working with a passionate cross-functional team.
Requirements
- Bachelor’s degree in life sciences, engineering, or related field
- 5+ years of clinical research experience (device experience strongly preferred)
- Working knowledge of GCP (ICH E6), ISO 14155, and applicable FDA regulations
- Experience with electronic data capture (EDC) systems and clinical trial documentation
- Strong understanding of clinical trial processes, including monitoring and site management
- Excellent communication, organization, and problem-solving skills
- Ability to work independently in a fast-paced, evolving environment
Benefits
- Medical, dental, and vision insurance through a PPO plan
- Paid holidays
- Commuter benefits
- Meals provided
- 401(k) plan
- Parental leave
- Flexible time off