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Health Care 🏢 Full Time ⭐️ Verified

Senior Medical Director, Specialized Medicine (Rare Diseases)

ApexCare Medical Institute
Boston, MA
Salary Estimate
USD 180.000 – USD 250.000
Posting Time
5 Mei 2026
Deadline
5 Mei 2027

Job description

Join ApexCare Medical Institute, a leading center in specialized medicine focused on rare and underserved diseases. We are seeking a visionary Senior Medical Director to shape clinical strategy, drive high-impact programs, and elevate patient outcomes across national networks.

In this role, you will partner with cross-functional teams to translate cutting-edge science into patient-centered therapies, oversee clinical development, and mentor the next generation of medical leaders. This is a unique opportunity to influence care pathways, advance translational research, and contribute to a culture of excellence and innovation.

We offer a competitive compensation package, comprehensive benefits, and a collaborative environment dedicated to advancing specialized medicine and improving lives.

Responsibility

  • Lead clinical strategy for rare disease programs, align with organizational goals and patient needs.
  • Direct multi-disciplinary teams across clinical development, medical affairs, and patient advocacy.
  • Design, oversee, and monitor clinical trials and real-world studies; ensure data integrity and safety.
  • Collaborate with R&D, regulatory, and commercial teams to translate science into patient-centered solutions.
  • Champion patient safety, ethics, and regulatory compliance (FDA/ICH-GCP).
  • Mentor physicians and healthcare professionals; foster professional development and succession planning.
  • Represent the organization at conferences, advisory boards, and external collaborations.

Qualification

  • MD or DO with board certification in Internal Medicine, Endocrinology, Medical Genetics, or equivalent; fellowship in rare diseases preferred.
  • Minimum of 7 years of clinical leadership experience and program development in specialized medicine.
  • Proven track record in rare disease programs, clinical trials, and translational research.
  • Strong regulatory and ethical knowledge (FDA, ICH-GCP, compliance frameworks).
  • Excellent strategic thinking, communication, and stakeholder management skills.
  • Experience building and leading high-performing teams and partnerships with academia and industry.
  • Fluent in data-driven decision making and medical writing for regulatory submissions.

Required Skills

Clinical leadership Rare disease program development Clinical trial design Regulatory affairs Multi-disciplinary team leadership Medical writing Stakeholder engagement Data analysis Evidence-based medicine

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