United States onlyWe are seeking a Senior CRA to lead site monitoring activities, while also supporting a broad range of clinical responsibilities, including process development, in-house operations, and study oversight.
Requirements
- Extensive experience in clinical research preferably in medical devices
- Extensive on-site and remote monitoring experience
- Experience developing or supporting SOPs, WIs, and process documentation.
- Strong understanding of GCP, ICH, FDA, and global clinical research guidelines.
- Proficiency with EDC, eTMF, CTMS, and standard office software.
- Strong communication and relationship-building skills at both site and sponsor levels.
- Ability to prioritize effectively and manage multiple responsibilities.
- Excellent organizational and documentation skills with attention to detail.
Benefits
- Company equity plan
- Annual Unlimited PTO
- Health insurance plan - CoMind contributes 50% to the monthly premium (with the Blue Cross Network)
- Dental insurance (50% Employer Contributions to individual policy)
- Vision insurance (50% Employer Contributions to individual policy)
- 401k plan with an employer match up to 3%
- Mental health resources
