Director, Medical Affairs — Launch Readiness

Initial Therapeutics, Inc.

South San Francisco (CA)

Hybrid

USD 200,000 - 250,000

Full time

14 days+
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Benefits offered by this job

Stock options
Annual bonus program
Health insurance premiums paid

Job summary

Alumis Inc. seeks a Medical Director to lead Medical content strategy, scientific readiness, and launch execution.

You will translate emerging clinical data into accurate, clinically meaningful resources for internal teams and external scientific engagement. Based in South San Francisco, CA, this role involves cross-functional partnership acrossClinical Development, Medical Information, Regulatory, and Field Medical to ensure consistency from late-stage development through commercialization.

Qualifications

  • Ability to translate complex clinical data into educational content.
  • Experience leading MLR reviews for promotional and non-promotional materials.
  • Track record developing launch-ready medical content and field resources.
  • Excellent scientific writing and presentation skills.
  • Strong project leadership across cross-functional teams.

Responsibilities

  • Serve as Medical Affairs lead for Medical Review of materials.
  • Lead medical content strategy and scientific readiness for launch.
  • Develop field-facing medical resources and educational materials.
  • Coordinate training, congresses, and data disclosures.
  • Collaborate with Regulatory, Commercial, Legal, and Field Medical teams.

Skills

Medical Affairs leadership
Scientific writing
Cross-functional collaboration
MLR review experience
Launch readiness
Strategic thinking

Education

MD/DO/PhD or equivalent

Tools

MS Office
PowerPoint

Job description

Alumis Inc. seeks a Medical Director to lead Medical content strategy, scientific readiness, and launch execution.

You will translate emerging clinical data into accurate, clinically meaningful resources for internal teams and external scientific engagement. Based in South San Francisco, CA, this role involves cross-functional partnership acrossClinical Development, Medical Information, Regulatory, and Field Medical to ensure consistency from late-stage development through commercialization.

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