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About the Role:
- Management and operational delivery of clinical elements within trials including site selection, start-up, enrollment management, and close-out.
- Ensure appropriate communication, regulatory documentation, and ongoing oversight by collaborating with functional team members.
- Lead CRAs to establish high-quality site relationships and oversee monitoring, regulatory, IP, and site payment activities.
About You:
- You have responsibility and a say in how clinical trials are run, with a consultative approach to trial management.
- You are well-organized, flexible, and able to manage timelines and shifting priorities without sacrificing quality.
- You thrive with autonomy and ownership to deliver successful outcomes, identifying risks and handling them resolutely.
Qualifications:
- Bachelor's degree or equivalent in science/health, with experience in oncology.
- Demonstrable experience leading clinical aspects across multiple countries in a CRO/pharma/biotech.
- Knowledge of GCP/ICH guidelines and clinical development process, with proficiency in MS Office and clinical software.
Precision for Medicine
Precision for Medicine is a precision medicine CRO that combines novel clinical trial designs, biomarker and data analytics, with a focus on rare diseases and oncology. The company is part of Precision Medicine Group, a growing organization dedicated to advancing oncology development and positively impacting patient health.