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Medical Director of Oncology Clinical Research
2 months ago
Tanner & Associates is seeking a highly skilled Medical Director of Oncology Clinical Research to join our team. As a key member of our organization, you will be responsible for leading the design, implementation, and analysis of clinical trials in the oncology field.
Key Responsibilities- Design and Implementation: Develop and execute clinical trial protocols, working closely with cross-functional teams to ensure successful trial execution.
- Medical Monitoring: Provide medical oversight and monitoring of clinical trials, ensuring compliance with ICH/GCP guidelines.
- Data Analysis and Interpretation: Analyze and interpret clinical trial data, presenting findings to stakeholders and contributing to the development of strategic clinical trial plans.
- Collaboration and Communication: Build and maintain relationships with external partners, including clinical investigators, advisors, and regulatory authorities.
- Education: M.D. with board certification/eligibility in hematology/oncology, or a PhD/PharmD with at least 5 years of drug development experience.
- Experience: Prior experience with clinical trials in an oncology-related field, with a strong understanding of the clinical trial process and compliance requirements.
- Skills: Excellent technical understanding of oncology, clinical trial design, and data analysis, as well as strong written and verbal communication skills.
Tanner & Associates offers a dynamic and challenging work environment, with opportunities for professional growth and development. If you are a motivated and experienced Medical Director of Oncology Clinical Research, we encourage you to apply for this exciting opportunity.
