Senior Medical Director, Clinical Development (Rheumatology)

Avalo Therapeutics

Chesterbrook (PA)

On-site

USD 250,000 - 360,000

Full time

14 days+

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Job summary

Avalo Therapeutics is seeking a Medical Director to guide clinical development from early trials through regulatory approval, focusing on rheumatoid and immune-mediated inflammatory diseases. You will coordinate with operations, regulatory, biomarker teams, and CROs to ensure efficient trial execution in a fast-paced environment.

Ideal candidates have 5+ years in biotech/pharma development, with direct experience in phase 2/3 studies and a background in biologics.

Qualifications

  • MD or equivalent medical degree required.
  • Minimum 5+ years of biotech/pharma/clinical development experience.
  • Direct experience leading late-stage (2/3) drug development.
  • Experience with biologics desirable.
  • Strong understanding of early development, dose escalation, safety monitoring.

Responsibilities

  • Provide medical leadership for assigned clinical program(s).
  • Contribute to early clinical development strategy including dose selection and trial design.
  • Support design and regulatory documents in compliance with GCP and GMP.
  • Serve as Medical Monitor for ongoing studies and review safety data.
  • Collaborate with CROs and external vendors to ensure high-quality study execution.
  • Prepare medical writing for study reports and labeling.

Skills

Medical leadership
Clinical development strategy
Regulatory submissions
Safety monitoring
Biomarker strategy

Education

MD or equivalent medical degree

Tools

ICH-GCP familiarity

Job description

Avalo Therapeutics is seeking a Medical Director to guide clinical development from early trials through regulatory approval, focusing on rheumatoid and immune-mediated inflammatory diseases. You will coordinate with operations, regulatory, biomarker teams, and CROs to ensure efficient trial execution in a fast-paced environment.

Ideal candidates have 5+ years in biotech/pharma development, with direct experience in phase 2/3 studies and a background in biologics.

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