Description
Entry-level Clinical Research Associates assist in monitoring clinical trials and ensuring compliance with study protocols. They work under supervision to support trial operations at Australian sites.
Responsibilities
- Assist in site selection, initiation, and monitoring visits.
- Verify data accuracy and adherence to trial protocols.
- Support ethics and regulatory submissions.
- Report any protocol deviations to senior staff.
- Maintain study files and documentation.
Qualifications
- Bachelor’s degree in life sciences or healthcare.
- Knowledge of clinical trial processes and GCP.
- Strong attention to detail and willingness to learn.
- Effective communication and interpersonal skills.
