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Health Care 🏢 Full Time ⭐️ Verified

Senior Medical Director, Specialized Medicine

NovaCura Therapeutics
Boston, MA
Salary Estimate
USD 140.000 – USD 210.000
Posting Time
7 Mei 2026
Deadline
7 Mei 2027

Job description

Join NovaCura Therapeutics, a leader in Specialized Medicine focused on rare and complex disease areas. We are seeking a strategic, data-driven Medical Director to guide clinical programs, translational research, and cross-functional collaboration.

In this role, you will shape clinical development plans, oversee investigator engagement, ensure the highest standards of patient safety, and drive innovation from bench to bedside.

Responsibility

  • Lead the design and execution of late-stage clinical development strategies for rare diseases and specialized therapies.
  • Collaborate with R&D, Biostatistics, Medical Affairs, and Regulatory to define endpoints, risk-benefit, and development plans.
  • Oversee investigator-initiated studies, site selection, and clinical trial operations in collaboration with CROs.
  • Ensure compliance with regulatory requirements (FDA/EMA) and safety monitoring; lead safety reviews.
  • Mentor and develop a high-performing medical affairs team; represent the company at medical conferences.
  • Drive publication strategy and medical communications; author or co-author pivotal trial protocols and manuscripts.
  • Build and maintain relationships with payer, patient advocacy groups, and key opinion leaders.

Qualification

  • MD, DO, or PhD in life sciences; board certification in a relevant clinical specialty preferred.
  • 8+ years of experience in clinical development, medical affairs, or related field with leadership experience in Rare Diseases/Specialized Medicine.
  • Strong knowledge of regulatory requirements (FDA, EMA) and pharmacovigilance practices.
  • Proven track record in protocol design, publication planning, and investigator engagement.
  • Excellent communication, presentation, and cross-functional leadership skills.
  • Ability to thrive in a fast-paced biotech environment with demonstrated strategic thinking and execution.
  • Willingness to travel 20-30% and work across global teams.

Required Skills

Clinical development rare diseases pharmacovigilance medical writing protocol development investigator relations data analysis FDA/EMA regulatory knowledge trial management systems

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