Job Summary
The Clinical Research Associate I for the Microbiome Program will play a pivotal role in advancing innovative research initiatives. This position, located in Duarte, California, entails responsibilities related to the accurate execution and documentation of clinical protocols, while ensuring compliance with established safety practices.
Responsibilities
- Ensure accurate documentation of clinical protocols.
- Communicate pertinent changes to investigators effectively.
- Collaborate with physicians or nurses to facilitate protocol-related testing.
- Maintain adherence to safety practices throughout the clinical research process.
Qualifications
- Strong attention to detail with excellent organizational skills.
- Ability to work collaboratively with clinical staff and investigators.
- Knowledge of clinical trial procedures and protocol adherence.
- Effective communication skills for documentation and reporting.
