Job Summary
The Clinical Research Associate (CRA) plays a pivotal role in the management and oversight of clinical trials. This position is crucial for ensuring that the research conducted adheres to regulatory guidelines and meets high standards of quality. The CRA will be responsible for monitoring clinical trial sites and ensuring that all aspects of the study are executed in compliance with protocols and regulations.
Responsibilities
- Monitor clinical trial sites for regulatory compliance and protocol adherence.
- Conduct site initiation, monitoring, and close-out visits.
- Ensure the accurate collection and verification of trial data.
- Maintain effective communication with site staff and stakeholders.
- Assist in the preparation of study-related documents and reports.
- Provide training and guidance to site personnel regarding study procedures.
Qualifications
- Bachelor’s degree in life sciences or a related field.
- Proven experience in clinical research, preferably in a CRA role.
- Strong knowledge of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent organizational and communication skills.
- Ability to manage multiple priorities and work independently.
