Senior Clinical Biomarker Strategy Lead

Biogen

San Francisco (CA)

Hybrid

USD 161,000 - 222,000

Full time

14 days+

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Benefits offered by this job

Medical, Dental, Vision
401(k) with company match
Stock purchase plan
Tuition reimbursement

Job summary

Biogen is seeking an Associate Director, Clinical Biomarkers Lead to drive comprehensive biomarker strategies across immunology and neuromuscular programs. The role includes oversight of biomarker development, data generation and interpretation, and mentorship of the biomarker team within a hybrid San Francisco setting.

Collaboration with research, regulatory, medical affairs, and external partners is essential.

Qualifications

  • PhD with 10+ years in industry and biomarker leadership.
  • Experience leading/implementing clinical biomarker strategies in immune-mediated diseases.
  • Strong communication, manuscript/reports and regulator interactions.

Responsibilities

  • Develop and implement comprehensive biomarker strategies for clinical programs.
  • Drive generation, analysis, and interpretation of biomarker data in studies.
  • Provide mentorship on biomarker strategy development and implementation.
  • Coordinate biomarker activities across research, clinical development, regulatory, and medical affairs.
  • Manage external collaborators and CROs for assay development and outsourced projects.
  • Author/review clinical protocols, medical affairs, and regulatory documents.

Skills

PhD + 10+ yrs
Biomarker strategy leadership
Cross-functional leadership
Regulatory interaction experience
Clinical biomarker technologies
Flow cytometry & immunoassays

Education

PhD

Tools

Flow cytometry
Immunoassay platforms

Job description

Biogen is seeking an Associate Director, Clinical Biomarkers Lead to drive comprehensive biomarker strategies across immunology and neuromuscular programs. The role includes oversight of biomarker development, data generation and interpretation, and mentorship of the biomarker team within a hybrid San Francisco setting.

Collaboration with research, regulatory, medical affairs, and external partners is essential.

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