Remote Associate Medical Director, Rare Neurology Outcomes

Biogen, Inc.; United States; Hybrid; USD 184,000 - 253,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

Tuition reimbursement

Bonus and equity opportunities

Paid time off and holidays

Job summary

Biogen, Inc. seeks an Associate Medical Director, Rare Neurology Outcome Development to lead development and implementation of innovative outcome measures across our Rare Neurology portfolio.

You will help qualify biomarkers and digital endpoints, and generate evidence across the product lifecycle in collaboration with cross-functional teams. You will contribute to study design, data interpretation, and communications with regulators, investigators, and stakeholders, aligning evidence plans with

Qualifications

• Experience in clinical outcome assessment strategy and implementation.
• Knowledge of endpoint development and qualification for clinical trials.
• Ability to analyze and interpret clinical trial data.
• Strong project management in a fast-paced, global matrix environment.

Responsibilities

• Support development and implementation of novel outcome measures (biomarkers, digital endpoints).
• Contribute to evaluation and refinement of existing measures using internal/external data.
• Design and execution of outcome development studies and natural history studies.
• Collaborate with internal/external experts to advance patient-centered outcome measurement.
• Support integrated evidence plans and regulatory interactions.

Skills

Clinical research

Outcome development

Cross-functional collaboration

Regulatory knowledge

Biostatistics

GCP proficiency

Education

Ph.D./MD/PharmD

Job description

Biogen, Inc. seeks an Associate Medical Director, Rare Neurology Outcome Development to lead development and implementation of innovative outcome measures across our Rare Neurology portfolio.

You will help qualify biomarkers and digital endpoints, and generate evidence across the product lifecycle in collaboration with cross-functional teams. You will contribute to study design, data interpretation, and communications with regulators, investigators, and stakeholders, aligning evidence plans with