Senior Medical Director, Clinical Development — Hybrid & Impact

BioSpace

Cambridge (MA)

Híbrido

USD 293 000 - 380 000

Tempo integral

Há 9 dias

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

Ultrapassa os filtros ATS

Vantagens oferecidas por esta oferta de emprego

Hybrid schedule
Health benefits
Equity incentive

Resumo da oferta

Beeline Medicines seeks a Senior Medical Director, Clinical Development to lead medical strategy for inflammation programs. You will own development plans across Phase I–III, mentor junior physicians, and influence portfolio decisions.

The role blends hands-on program leadership with cross‑functional collaboration in a growth-stage biopharmaceutical setting. You will interact with regulators and key opinion leaders, drive study design, medical monitoring, and risk management, and contribute to

Qualificações

  • MD/DO required with strong rheumatology/immunology training.
  • Minimum 10 years clinical/pharma/biotech experience; 5+ years in development.
  • Hands-on protocol development, medical monitoring, and regulatory submission experience.

Responsabilidades

  • Serve as physician lead for clinical development programs across I–III phases.
  • Design and review protocols, IBs, informed consent, and regulatory submissions.
  • Provide medical oversight of trials: safety monitoring and risk assessment.

Conhecimentos

MD/DO
Rheumatology
Clinical development
Regulatory submissions
KOL relationships

Formação académica

Advanced clinical degree (MD/DO)
Board certification in rheumatology/immunology
PhD/MPH/MBA (plus)

Descrição da oferta de emprego

Beeline Medicines seeks a Senior Medical Director, Clinical Development to lead medical strategy for inflammation programs. You will own development plans across Phase I–III, mentor junior physicians, and influence portfolio decisions.

The role blends hands-on program leadership with cross‑functional collaboration in a growth-stage biopharmaceutical setting. You will interact with regulators and key opinion leaders, drive study design, medical monitoring, and risk management, and contribute to

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