Director, Scientific Communications & Medical Information

About the position

The Director of Scientific Communications & Medical Information at Meitheal Pharmaceuticals is responsible for leading the strategic development, implementation, and execution of scientific communication and medical information activities. This role is critical in ensuring that internal and external stakeholders receive timely, accurate, and impactful scientific information across all therapeutic areas, specifically focusing on Meitheal’s infectious disease portfolio, including CONTEPO (IV Fosfomycin) and XENLETA (IV and oral Lefamulin acetate), oncology and other biosimilar immunologic therapies, and numerous pipeline assets, some of which may include E.U. and other ex-U.S. territories.

Responsibilities

• Lead the development and execution of scientific communication and medical information strategies for Meitheal’s product portfolio.
• Oversee the integration of Medical Information, Publications, and Scientific Communications into a high-performing, compliant department.
• Develop and implement a comprehensive publication strategy for all assigned therapeutic areas and products.
• Ensure publication strategies are data-driven, scientifically rigorous, and compliant with regulatory guidelines.
• Collaborate with clinical, regulatory, and medical affairs team members to ensure publications align with clinical development milestones.
• Lead cross-functional teams in the development, writing, editing, and submission of high-quality scientific manuscripts.
• Build and maintain strong relationships with KOLs, investigators, journal editors, and congress organizers.
• Develop and implement a medical information strategy that supports Meitheal’s products.
• Oversee the operation of Medical Information Call Centers.
• Develop and implement KPIs to monitor the effectiveness of Medical Information services.
• Establish and enforce policies and procedures to ensure compliance with regulatory requirements.

Requirements

• Minimum of 10+ years of experience in the biotech/pharmaceutical industry.
• 4+ years background in Scientific Communications and Medical Information.
• Proven experience managing cross-functional teams in an organization.
• Sound understanding of the drug development process.
• Experience with regulatory compliance and industry standards governing scientific communication.
• Advanced scientific or medical degree (R.Ph., Ph.D., equivalent) strongly preferred.
• Strong leadership and strategic thinking skills.
• Excellent communication skills, both verbal and written.
• Demonstrated ability to manage complex projects and solve problems in a matrix environment.
• In-depth understanding of regulatory guidelines and compliance requirements.
• Ability to travel up to 25% domestically.

Benefits

• Hybrid Work Schedule (Preferred): Enjoy the flexibility to work remotely three days a week.
• Casual Dress Code: Embrace a relaxed and comfortable dress code.
• Collaborative Culture: Join a team that values open communication and teamwork.
• Professional Growth: Ample opportunities for professional development and career advancement.