Associate Medical Director, Regulatory Affairs

2 days ago


Cambridge, Cambridgeshire, United Kingdom Sobi group Full time

Join Sobi's Team: We are seeking an experienced Associate Medical Director, Regulatory Affairs to join our team of experts in clinical development and regulatory affairs.

About the Role: The successful candidate will be responsible for leading clinical development activities, providing scientific and medical input to clinical study documents, and collaborating with regulatory and reimbursement authorities.

Key Responsibilities:

  • Plan, design, conduct, and report Sobi-sponsored studies.
  • Provide clinical, medical, and strategic input to clinical development plans.
  • Collaborate with cross-functional teams to ensure compliance with regulatory requirements.

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. Proven self-management skills and proficiency in English required.

Salary: $130,000 - $170,000 per year, based on experience and qualifications.

Benefits: Competitive benefits package, emphasis on work-life balance, opportunities for professional growth, diversity and inclusion, and making a positive impact on the lives of people with rare diseases.



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