Clinical Trial Manager

About the Role:

• Manage and deliver clinical elements of trials across multiple countries, including site selection and start-up.
• Lead CRAs and oversee monitoring, regulatory documentation, and site correspondence.
• Identify challenges and provide creative action plans to ensure timeline adherence and quality.

Qualifications:

• Bachelor's degree in science or health-related field with oncology experience.
• Demonstrable experience leading clinical aspects of studies in a CRO, pharma, or biotech company.
• Working knowledge of GCP/ICH guidelines and clinical development process.

Skills and Competencies:

• Demonstrated computer skills including MS Office, MS Project, CTMS, eTMF, EDC, and IXRS.
• Ability to develop positive working relationships with internal and external organizations.
• Mastery of ICH-GCP, regulatory guidance, and medical terminology.

Why Precision for Medicine:

• Revolutionizing cancer treatment with precision medicine, targeting tumors at the molecular level.
• Combining deep science with advanced data platforms for real-time decisions.
• Dedicated to positively impacting patients' lives through specialized oncology development.