Associate Medical Director, Clinical Development, Neuromuscular

Biogen

Cambridge, MA, United States
Base: $194,000.00-$267,000.00; bonus/equity: short...
Neuromuscular programs
Clinical trial design and execution
Biomarkers and clinical endpoints
The Neuromuscular Development Unit at Biogen is accountable for developing ground-breaking therapies in Spinal Muscular Atrophy (SMA), Amyotrophic Lateral Sclerosis (ALS), and muscle diseases from early to late-stage clinical development

Job Summary

  • The Neuromuscular Development Unit at Biogen is accountable for developing ground-breaking therapies in Spinal Muscular Atrophy (SMA), Amyotrophic Lateral Sclerosis (ALS), and muscle diseases from early to late-stage clinical development.
  • As a member of the team, the associate medical director will work on early- and/or late-stage ALS programs and potentially contribute to other programs.
  • Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being.

Matching Summary

The Neuromuscular Development Unit at Biogen is accountable for developing ground-breaking therapies in Spinal Muscular Atrophy (SMA), Amyotrophic Lateral Sclerosis (ALS), and muscle diseases from early to late-stage clinical development.

Salary

Base: $194,000.00-$267,000.00; Bonus/Equity: Short term and long-term incentives, cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, Life insurances, Fitness & Wellness programs, Disability insurance, Paid time off, Holidays, Paid Maternity and Parental Leave, 401(k) match, ESPP, Tuition reimbursement

Skills & Requirements

Must-have

  • Neuromuscular programs
  • Clinical trial design and execution
  • Biomarkers and clinical endpoints
  • Regulatory submissions and interactions

Nice-to-have

  • Global therapeutic unit advancement
  • Highly matrixed environment collaboration
  • Pioneering spirit and commitment to excellence

Key Requirements

  • MD, Ph.D., and/or PharmD
  • At least 5 years clinical research experience
  • Clinical data analysis and interpretation
  • Working knowledge of biostatistics
  • GCP and regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter