Clinical Research Associate
Job Summary
Working remotely in a full-time capacity, the Clinical Research Associate will manage clinical trial activities, ensuring compliance with regulatory requirements and maintaining data integrity throughout the study lifecycle.
Key responsibilities
- Oversee the execution of clinical trials, including site selection, initiation, monitoring, and closeout activities
- Ensure adherence to Good Clinical Practice (GCP) guidelines and regulatory standards
- Collaborate with cross-functional teams to facilitate project timelines and deliverables
Required qualifications
- Bachelor's degree in a related field, such as life sciences or nursing
- Minimum of 2 years of experience in clinical research or a related area
- Knowledge of clinical trial regulations and GCP guidelines
- Experience with data management and clinical trial management systems
- Certification as a Clinical Research Associate (CRA) is preferred but not required
Complete Job Description
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