Associate Medical Director, Rare Neurology Outcome Development

Biogen; United States; On-site; USD 180,000 - 280,000; Full time

Job summary

Scorpion Therapeutics is seeking an Associate Medical Director for Rare Neurology Outcome Development to lead the design and validation of innovative outcome measures for rare neurological diseases, including neuromuscular conditions. This role combines scientific rigor with regulatory insight to advance early- and late-stage assets.

You will partner with clinical and translational science teams, shape study endpoints and evidence-generation plans, contribute to publications and conference

Qualifications

• Ph.D., MD, or PharmD required.
• 5+ years in clinical research or outcome measure development.
• Experience in clinical outcome assessment strategy, trial design, and data interpretation.
• Strong knowledge of GCP, biostatistics, and regulatory standards.
• Excellent project management and stakeholder engagement skills.

Responsibilities

• Develop, evaluate, and refine biomarkers, digital endpoints, and clinical outcome assessments.
• Contribute to outcome studies, natural history research, and regulatory interactions.
• Support evidence generation frameworks for early-stage assets.
• Collaborate with cross-functional teams, external experts, and stakeholders.
• Contribute to scientific publications and conference presentations.

Skills

Clinical outcome measurement

Trial design

Data interpretation

GCP knowledge

Biostatistics

Regulatory standards

Project management

Stakeholder engagement

Education

Ph.D., MD, or PharmD

Job description

Role: Associate Medical Director, Rare Neurology Outcome Development, supporting innovative outcome measures and evidence generation strategies for rare neurological diseases, including neuromuscular conditions.

Responsibilities

• develop, evaluate, and refine biomarkers, digital endpoints, and clinical outcome assessments;
• contribute to outcome studies, natural history research, and regulatory interactions;
• support evidence generation frameworks for early-stage assets;
• collaborate with cross-functional teams, external experts, and stakeholders;
• contribute to scientific publications and conference presentations.

Requirements

• Ph.D., MD, or PharmD;
• 5+ years in clinical research or outcome measure development;
• experience in clinical outcome assessment strategy, trial design, and data interpretation;
• strong knowledge of GCP, biostatistics, and regulatory standards;
• excellent project management and stakeholder engagement skills.

Preferred Qualifications

• experience with biomarkers, wearables, digital health, neurology/rare diseases, and pipeline/portfolio strategy.

High-Value Biopharma Specifics

focus on neurology, rare disorders, biomarker and digital endpoint development, clinical trial support, and evidence generation; involvement in early to late-stage development; occasional domestic and international travel.

Work Setup

not specified; team-based, global environment.