
cra ii
3 weeks ago
- Conduct and report all types of on-site monitoring visits
- Participate in site feasibility, selection, and study start-up
- Perform CRF review, SDV (Source Data Verification), and query resolution
- Facilitate site budget and contract negotiations
- Track trial progress and enrollment at the country level
- Maintain communication with sites, vendors, and internal project teams
- Act as the main point of contact for in-house support services
- Participate in feasibility research and support document preparation for submissions
- Bachelor's degree in Life Sciences, Pharmacy, Nursing, or equivalent
- ~2 years of independent on-site monitoring experience in Australia (slightly less may be considered)
- Solid experience in monitoring visits across Phases II and/or III
- Knowledge of study start-up and feasibility assessment is preferred
- Therapeutic area experience in IBD, Oncology, or Infectious Diseases is an advantage
- Full working proficiency in English
- Proficient in MS Office (Word, Excel, PowerPoint)
- Strong planning, multitasking, communication, and problem-solving skills
- Willingness to travel as required
Permanent, full-time
LocationSydney
How to applyPlease click 'apply' or contact Steven Fan (Recruiter, APAC) at Planet Pharma for more information:
T: +61 370427282
Planet Pharma is an Equal Opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.
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