Clinical Development Program Lead

3 weeks ago


Cambridge, Cambridgeshire, United Kingdom Sobi group Full time

About the Company: Sobi is dedicated to developing and delivering innovative therapies to improve the lives of people with ultra-rare diseases.

Salary Range: $120,000 - $160,000 per year, based on experience and qualifications.

Job Summary: As an Associate Medical Director, Regulatory Affairs, you will be responsible for planning, designing, conducting, and reporting Sobi-sponsored studies. You will collaborate with cross-functional teams to provide clinical, medical, and strategic input to clinical development plans.

Key Responsibilities:

  • Provide high-quality scientific and medical input to clinical study documents.
  • Collaborate with regulatory and reimbursement authorities to provide strategic and operational clinical development expertise.
  • Contribute to the delivery of clinical parts of submissions and other regulatory documents.

Requirements: A medical degree, at least 3-4 years of clinical experience, or 4-5 years of solid record of accomplishment within rheumatology/immunology drug development programs. Proficient level of English required.

Benefits: Competitive benefits package, work-life balance, opportunities for professional growth, diversity and inclusion, and making a positive impact on rare disease patients.



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