Senior Director, North American Field Medical Affairs

The Sr. Director, US Medical Science Liaison will serve as scientific and clinical expert, identifying and building trusted relationships with KOLs and ECP advocates, and identifying / supporting opportunities for clinical trials.

The role is responsible for leading and overseeing the field-based medical science liaison team within the Medical Affairs department. This position plays a critical role in building scientific relationships with key opinion leaders, supporting strategic medical objectives, and disseminating up-to-date clinical and scientific information to healthcare professionals. The ideal candidate will collaborate cross-functionally to ensure alignment with organizational goals while maintaining the highest standards of scientific integrity and compliance. Skills: 

• Strong scientific and clinical knowledge in relevant therapeutic areas
• Excellent communication and presentation skills
• Ability to build and maintain relationships with key opinion leaders and healthcare professionals
• Strategic thinking and problem-solving abilities
• Leadership and team management experience
• Proficiency in interpreting and disseminating complex clinical data
• High level of integrity and commitment to compliance
• Effective cross-functional collaboration skills
• Adaptability in a fast-paced and evolving environment
• Strong organizational and project management skills

 
Experience: 
Minimum of 10 years of experience in the pharmaceutical, biotechnology, or healthcare industry, preferably in a medical affairs or clinical development role. Demonstrated track record of successfully collaborating with cross-functional teams and leading projects from inception to completion. Demonstrated experience working directly with key opinion leaders and managing external partnerships.   Prior experience managing MSLs.

Education: 
Advanced degree (MD, PharmD, PhD, or equivalent) in a relevant scientific or medical field is required. Additional certifications or training in clinical research, regulatory affairs, or medical affairs are considered an asset.

• Manage a team of MSLs across the US.
• Develop and implement medical strategies that align with overall business objectives.
• Interpret, communicate, and disseminate complex clinical and scientific data to internal and external stakeholders.
• Foster relationships with key opinion leaders, healthcare professionals, and external partners to support medical initiatives.
• Ensure compliance with all relevant regulations, policies, and ethical standards in all medical affairs activities.
• Lead and contribute to cross-functional teams to drive project success from initiation through completion.
• Support the design, execution, and reporting of clinical trials and research studies.
• Provide medical expertise for regulatory submissions, promotional materials, and educational programs.
• Identify and address unmet medical needs through evidence generation and strategic insights.
• Maintain up-to-date knowledge of industry trends, scientific advancements, and competitive landscape.
• Contribute to the professional development and training of team members and colleagues.

• Competitive salary and benefits package.
• Opportunities for professional development and career growth.
• Collaborative and innovative work environment.