Job Summary
The Clinical Research Associate (CRA) plays a crucial role in the management and oversight of clinical trials. This position is responsible for ensuring compliance with regulatory standards, protocol adherence, and maintaining the integrity of trial data. The CRA will work collaboratively with clinical trial sites, monitor study progress, and communicate findings to stakeholders to facilitate successful trial outcomes.
Responsibilities
- Monitor clinical trial sites to ensure compliance with protocols and regulatory requirements.
- Perform site initiation, monitoring, and close-out visits.
- Review and verify the accuracy of clinical data collected.
- Facilitate effective communication between study teams, investigators, and sponsors.
- Assist in the development and maintenance of study documentation.
- Provide training and support to site personnel on study protocols and procedures.
- Identify and address issues at trial sites proactively.
Qualifications
- Bachelor’s degree in a life science or related field is required.
- Experience in clinical research or a related field is preferred.
- Strong understanding of Good Clinical Practice (GCP) and regulatory guidelines.
- Excellent organizational and communication skills.
- Ability to work independently and manage multiple tasks effectively.
- Willingness to travel as needed for site visits.
