
Baselga Cancer Research Scholar
- Mississauga, ON
- Permanent
- Full-time
- Serving as medical monitor with primary responsibility for patient safety and conduct of assigned trials as well as overall data interpretation and safety surveillance
- Establishing and approving scientific methods for design and implementation of applicable clinical protocols, data collection systems, and final reports
- Assisting in design of clinical development plans and overall strategy for compounds, therapeutic classes of compounds or indications in light of developments in the area of clinical and pharmaceutical oncology
- Collaborating with pre-clinical and translational sciences, and senior management in assessing requirements for emerging products
- Participating in the selection and management activities of CROs
- Supervising project team members in planning, conducting and evaluating clinical trials
- Planning and managing investigator meetings, advisory boards and other scientific committees
- Patient safety
- Clinical operations
- Regulatory affairs
- Biostatistics
- Medical affairs
- Translational medicine or precision medicine
- Experience in molecular oncology and/or translational science
- Medical specialty and sub-specialty training and Board Certification
- Excellent oral and written skills, strong interpersonal and listening skills
- Results driven to achieve creative and sound outcomes
- Proven leadership skills and demonstrated ability to interact collaboratively in a cross-functional environment.
- Ability to make sound and timely decisions; agile in learning and action oriented
- High level of emotional intelligence; able to deal with ambiguity
- Able to relate to varied level audiences across the organization; able to set priorities for team and maintain accountability; skilled in negotiating organizational boundaries and hierarchy; able to build effective teams