
On-Site Monitoring Specialist
7 days ago
We are seeking a detail-oriented and organized Clinical Research Associate II to conduct on-site monitoring visits, perform CRF reviews, and facilitate site budget and contract negotiations.
The ideal candidate will have solid experience in monitoring visits across Phases II and/or III, with a strong understanding of study start-up and feasibility assessment. Therapeutic area experience in IBD, Oncology, or Infectious Diseases is an advantage.
Key Qualifications- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or equivalent
- ~2 years of independent on-site monitoring experience in Australia
- Proficient in MS Office (Word, Excel, PowerPoint)
- Strong planning, multitasking, communication, and problem-solving skills
- Conduct on-site monitoring visits
- Perform CRF reviews and SDV
- Facilitate site budget and contract negotiations
- Track trial progress and enrollment at the country level
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