Job Summary
The Senior Clinical Research Associate undertakes both remote and on-site monitoring of clinical study sites to guarantee adherence to compliance standards and the availability of necessary resources. This role involves offering guidance and training to less experienced staff while also aiding in the preparation and submission processes for regulatory and ethics committee documentation.
Responsibilities
- Conduct on-site and remote monitoring visits to verify site compliance and resource adequacy for clinical trials.
- Provide mentorship and training to junior clinical research personnel.
- Assist in the submissions to regulatory authorities and ethics committees.
Qualifications
- A college or university degree in Life Sciences is mandatory.
- Significant experience in on-site monitoring of phase 2/3 clinical trials is essential.
- Fluency in English is required for effective communication.
- The candidate must be willing to travel nationally as part of their job responsibilities.
