Associate Medical Director, Clinical Development, Neuromuscular

Biogen

Cambridge, MA, United States
Base: $194,000.00-$267,000.00; bonus/equity: cash ...
Clinical trial design and execution
Cross-functional team collaboration
Regulatory submissions and interactions
The Neuromuscular Development Unit at Biogen is accountable for developing ground-breaking therapies in Spinal Muscular Atrophy, Amyotrophic Lateral Sclerosis, 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, Amyotrophic Lateral Sclerosis, and muscle diseases from early to late-stage clinical development.
  • This role will drive the progression of a deep clinical portfolio and assist cross-functional teams in achieving innovative clinical trial designs, biomarkers, clinical endpoints, and regulatory interactions.
  • Biogen offers a full and highly competitive range of benefits including medical, dental, vision, life insurances, fitness programs, paid time off, parental leave, 401(k) with company match, and tuition reimbursement.

Matching Summary

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

Salary

Base: $194,000.00-$267,000.00; Bonus/Equity: Cash bonus and equity incentives available; Benefits: Medical, dental, vision, life insurance, paid vacation, parental leave, 401(k) match, tuition reimbursement

Skills & Requirements

Must-have

  • Clinical trial design and execution
  • Cross-functional team collaboration
  • Regulatory submissions and interactions
  • Clinical data analysis and interpretation
  • Project management skills
  • Knowledge of GCP and regulatory requirements

Nice-to-have

  • Effective communication skills
  • Ability to work in matrix environment
  • Experience with ALS clinical programs
  • Relationship building with stakeholders
  • Global thinking in therapeutic development

Key Requirements

  • MD, Ph.D., and/or PharmD degree
  • At least 5 years clinical research experience
  • Experience analyzing clinical safety and efficacy data
  • Working knowledge of biostatistics
  • Ability to travel domestically and internationally

Work Rights

Not specified

Tailored Resume

Cover Letter