As Chief Medical Officer for a cutting-edge oncology biotech, you will be the strategic leader overseeing the medical and clinical functions of the organization. This role requires thorough knowledge of oncology drug development, a passion for advancing cancer therapies, and the ability to ensure the highest standards of patient care and regulatory compliance.
Key Responsibilities
- Develop and execute the company’s clinical vision and strategy, aligning with corporate goals to advance our oncology pipeline.
- Lead clinical trials and other clinical research programs to bring innovative oncology therapies from development through regulatory approval.
- Work closely with research, regulatory, and commercial teams to ensure alignment on therapeutic goals and strategies.
- Ensure compliance with regulatory requirements (FDA, EMA, etc.) and ethical standards for all clinical activities.
- Oversee medical affairs to support product launches, develop clinical study protocols, and communicate data effectively to external stakeholders.
- Represent the company in industry forums, conferences, and medical meetings, and build relationships with key opinion leaders (KOLs) in oncology.
Objectives of This Role
- Drive clinical excellence in oncology care through innovative drug development and rigorous clinical trials.
- Build and nurture a high-performing clinical team, fostering an environment of continuous improvement.
- Align the medical strategy with company objectives, influencing product strategy and positioning in the oncology landscape.
- Leverage data analytics and emerging technologies to drive efficiencies in clinical operations.
- Maintain strong relationships with regulatory agencies, ensuring proactive compliance.
Essential Qualifications
- MD or equivalent, with specialization in oncology or hematology-oncology.
- Minimum of 10 years in oncology clinical development or a similar field, with 5+ years in a senior leadership role in the biotech/pharma sector.
- Proven track record in leading clinical trials, with in-depth knowledge of regulatory requirements for oncology drug development.
- Excellent verbal and written communication skills to articulate complex medical concepts to a range of audiences, including regulatory agencies, partners, and investors.
- Strong business acumen with the ability to contribute to long-term organizational planning and positioning.
Preferred Skills
- Advanced degree in public health, healthcare management, or a related field.
- Experience with data-driven decision-making, particularly in using analytics to improve clinical and operational efficiencies.
- Familiarity with digital transformation trends in healthcare and biotechnology.