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Position Summary:
- Responsible for the planning, conduct and oversight of the operational portion of clinical studies per defined scope of work.
- Ensures clinical studies are conducted in accordance with the protocol, SOPs, ICH-GCP and all applicable regulatory requirements.
Responsibilities:
- Collaborate with PM on monthly invoicing and variance management of clinical budget.
- Develop study related clinical documents (e.g. clinical plans, Informed Consent Form templates, study specific forms and manuals).
- Work closely with PM for project-specific resourcing issues.
Qualifications:
- Minimum of 5-8 years of clinical research experience or proven competencies for the position with significant clinical monitoring experience.
- Bachelor’s degree or equivalent combination of education/experience in science or health-related field.
- Oncology (Phase I) trial experience in Australia preferred
Precision for Medicine
Precision for Medicine integrates clinical trial execution with scientific knowledge, laboratory expertise, and data sciences to improve the speed, cost and success rate of bringing therapies to patients. They focus on Oncology and Rare Disease, providing deep scientific knowledge.