Description
Clinical Research Associates III serve as senior monitors, managing complex clinical trials and mentoring junior CRAs. They oversee site operations to ensure the success of Australian studies.
Responsibilities
- Lead site management activities for complex trials.
- Train and mentor junior CRAs.
- Address site-specific challenges and escalate issues as needed.
- Ensure high-quality data collection and documentation.
- Provide input on study design and operational strategies.
Qualifications
- Bachelor’s degree in life sciences or healthcare.
- 3+ years of clinical monitoring experience.
- Expertise in GCP and TGA requirements.
- Strong leadership and communication skills.
