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Senior Director, North American Field Medical Affairs

Hiring from
United States
Work type
Remote
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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.

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