Medical Director​/Senior Medical Director, Clinical Development

Transforming Lives with Breakthrough Therapies! At Lumos Pharma, we are on a mission to revolutionize the treatment of rare diseases. As a cutting-edge clinical-stage biopharmaceutical company, we are focused on developing innovative therapies where the need is greatest, and the science is clear. Our unwavering commitment is to bring safe, effective, and innovative treatments to patients through a strategy that values time and cost efficiency.

Join us in our pursuit of making a difference. Together, we can change the future of medicine!

The Medical Director/Senior Medical Director, Clinical Development – Endocrinology will provide scientific and clinical expertise to guide the development of innovative therapies for endocrine disorders. This individual will be instrumental in driving clinical development strategy, ensuring regulatory compliance, and advancing clinical trials from early through late stages. The role requires close collaboration with R&D, Regulatory, Commercial, and Market Access teams to optimize clinical trial design and implementation and enhance medical and scientific understanding in endocrinology.

• Lead the development of clinical strategies and plans for endocrine-related therapies, including clinical trial design, protocol development, and execution.
• Drive the scientific and clinical aspects of the clinical development program to ensure alignment with overall corporate and regulatory objectives.
• Oversee the planning and execution of Phase I-IV clinical trials in collaboration with cross-functional teams, ensuring that studies meet ethical and regulatory standards.

• Ensure successful trial execution, including protocol design, study feasibility, patient recruitment, data collection, and analysis.
• Collaborate with Clinical Operations to ensure adherence to trial timelines and budgets and proactively identify and address potential issues.
• Support data review and interpretation, providing critical insights for clinical reports and publications.

• Partner with Regulatory Affairs to prepare and review regulatory submissions (INDs, NDAs, MAAs) and provide clinical and scientific support for interactions with regulatory agencies, including the FDA, EMA, and other health authorities.
• Ensure that clinical programs comply with GCP, ICH, and other regulatory guidelines.

• Act as an endocrinology clinical and scientific expert for internal and external stakeholders, including opinion leaders, clinical investigators, and advisory boards, particularly within the endocrinology field.
• Communicate clinical trial results and product information to the medical community with development and delivery of scientific presentations, clinical study reports, and publications.
• Collaborate with the Medical Affairs team on post-approval studies, real-world evidence generation, and publication plans.

• Partner with R&D, Commercial, and Market Access teams to provide clinical input on product development, launch strategies, and lifecycle management of the endocrine portfolio.
• Work with Marketing and Commercial teams to support product differentiation, competitive positioning, and value proposition in the endocrinology market.
• Support patient advocacy and engagement activities.

• Establish and maintain strong relationships with key opinion leaders (KOLs), patient advocacy groups, and other external stakeholders in endocrinology.
• Represent the company at scientific and medical conferences and in medical advisory board meetings.

• Responsible for financial and compliance controls as they relate to my role. For example, being fiscally responsible in purchase decisions and completing compliance training in the specified time frames.

• Education:
  
  MD or equivalent with clinical experience and research in endocrinology
• Experience:
  
  Industry experience in clinical development (≥3 years for Medical Director; ≥5 years for Senior Medical Director);
  Strong, dedicated academic…