What are the responsibilities and job description for the Senior Director, Global Medical Affairs (Oncology) position at EPM Scientific?
We are seeking a highly skilled and experienced Senior Director, Global Medical Affairs (Oncology) to lead and develop our oncology medical affairs strategy on a global scale. The ideal candidate will possess a strong scientific background exceptional leadership abilities, and extensive knowledge of oncology therapeutics and clinical development. This role will be crucial in establishing and executing medical strategies to support our oncology portfolio, collaborating with cross-functional teams, and ensuring compliance with regulatory standards.
Key Responsibilities:
Lead the global medical affairs strategy for oncology, ensuring alignment with the company's overall business objectives and scientific goals.
Oversee the development and execution of medical plans, including clinical trials, publications, and scientific communications.
Collaborate with cross-functional teams, including R&D, regulatory affairs, and commercial operations, to provide medical expertise and support the development and commercialization of oncology products.
Establish and maintain strong relationships with key opinion leaders (KOLs), healthcare professionals, and external stakeholders to ensure the integration of medical insights into product development and marketing strategies.
Ensure compliance with regulatory requirements and industry standards in all medical affairs activities, including promotional materials, clinical trials, and medical communications.
Lead and manage a team of medical affairs professionals, providing mentorship, guidance, and development opportunities.
Monitor and analyze emerging trends, competitive intelligence, and scientific advancements in the oncology field to inform strategic decision-making.
Represent the company at scientific conferences, advisory boards, and industry events, presenting scientific data and sharing insights on oncology therapeutics.
Qualifications:
MD, PharmD, or PhD in a relevant scientific discipline, with extensive experience in oncology.
A minimum of 10 years of experience in medical affairs or related roles within the pharmaceutical or biotechnology industry.
Proven track record of successfully leading and managing global medical affairs teams and projects.
Strong understanding of oncology therapeutics, clinical development, and regulatory requirements.
Excellent communication and presentation skills, with the ability to engage and influence diverse stakeholders.
Demonstrated ability to think strategically, solve complex problems, and make data-driven decisions.
High ethical standards and a commitment to compliance with regulatory guidelines and industry best practices.
Willingness to travel domestically and internationally as needed.
If you are a strategic thinker with a passion for oncology and a desire to make a meaningful impact on patients' lives, we encourage you to apply for this exciting opportunity.
