
Senior Site Monitor
2 weeks ago
**Clinical Research Associate Role Overview**
">Job DescriptionClinical research associates play a vital role in the success of clinical trials. As part of our team, you will be responsible for site monitoring from selection to study close out, ensuring timely completion of milestones. You will work closely with site staff, PI, CTM, CTA, and contracts teams to deliver high-quality results.
Key Responsibilities:- Monitor the progress of assigned clinical trials and escalate protocol deviations, SAEs, and risks.
- Submit visit reports to the Clinical Trial Manager on time.
- Cross-functional collaboration is essential for delivering successful trials.
- Tertiary degree qualified in Life Sciences.
- 2+ years of independent site monitoring experience.
- Excellent communication and presentation skills are required.
A career with us comes with many benefits, including a competitive salary, annual leave entitlements, health insurance offerings, retirement planning, and an Employee Assistance Programme. Our inclusive culture values diversity and promotes well-being and work-life balance.
Our company is committed to equal opportunities and inclusion. If you need a reasonable accommodation during the application process or require assistance performing job duties, please let us know.
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