Job Summary
The Clinical Research Associate (CRA) plays a vital role in monitoring and overseeing clinical trials, providing essential support to ensure compliance with regulatory standards. This position is focused on maintaining integrity in data collection processes and advancing the development of medical products through diligent management of clinical research activities.
Responsibilities
- Conduct monitoring visits to study sites to ensure compliance with the study protocol and regulatory requirements.
- Review and verify the accuracy of data collected during clinical trials.
- Assist in the selection and initiation of clinical trial sites.
- Provide training and ongoing support to site staff regarding study protocols.
- Prepare detailed reports on site findings and communicate with project teams regarding any issues encountered.
- Assess the need for corrective action and facilitate the resolution of problems as needed.
Qualifications
- Bachelor’s degree in Life Sciences or a related field.
- Experience in clinical research or related activities is preferred.
- Strong understanding of Good Clinical Practice (GCP) and regulatory requirements.
- Excellent communication and interpersonal skills.
- Ability to work independently as well as part of a team.
- Detail-oriented with strong organizational skills and the ability to manage multiple tasks effectively.
