Senior Clinical Research Associate - Contract
Plan A Health · Los Angeles, CA · 3 wk ago
On-siteResearchContract
About the role
Responsible for overseeing clinical studies with a mix of remote monitoring and on-site visits, ensuring study quality and compliance.
Responsibilities
- Manage site engagement
- Monitor study progress
- Ensure adherence to regulatory standards and protocols
- Maintain detailed documentation to support clinical research outcomes
Qualifications & Skills
- Proven experience in CNS, oncology, or metabolic indications
- Strong understanding of regulatory standards
- Protocol compliance
- Effective site management
- Detail-oriented, proactive, and committed to quality
Key Attributes
- Collaboration
- Integrity
- Purpose-driven attitude
- Dedication to advancing clinical research