Clinical Research Director, Rare Disease

Sanofi

Cambridge, MA, USA
$206,250.00 - $343,750.00; not specified; not spec...
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Rare disease clinical development
Patient-centric focus
Gcp and regulatory compliance
** Sanofi is seeking a Clinical Research Director for Rare Disease programs, responsible for strategizing and executing clinical development while ensuring patient-centric approaches. The ideal candidate will hold an MD, have extensive experience in drug development, particularly in rare diseases, and possess strong leadership and communication skills. **

Job Summary

  • The Clinical Research Director (CRD), Rare Disease, is a senior scientific and clinical leader responsible for shaping and executing clinical development strategy for assigned rare disease programs — driving them from early development through registration with a patient-centric focus.
  • The CRD serves as a recognized scientific authority within the Rare Disease TA, championing clinical excellence, challenging conventional approaches, and advancing Sanofi's mission to deliver transformative therapies to underserved patients.
  • Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research.

Matching Summary

Match Score: 75

** Sanofi is seeking a Clinical Research Director for Rare Disease programs, responsible for strategizing and executing clinical development while ensuring patient-centric approaches. The ideal candidate will hold an MD, have extensive experience in drug development, particularly in rare diseases, and possess strong leadership and communication skills. **

Salary

$206,250.00 - $343,750.00; Not specified; Not specified

Skills & Requirements

Must-have

  • rare disease clinical development
  • patient-centric focus
  • GCP and regulatory compliance
  • biomarker identification
  • innovative trial designs

Nice-to-have

  • AI-powered research
  • transformative therapies
  • challenging conventional approaches
  • talent development

Key Requirements

  • MD required
  • 5+ years in drug development
  • experience with orphan drug frameworks
  • small patient population trial design
  • proven ability to lead cross-functional global teams

Work Rights

Not specified

Tailored Resume

Cover Letter