Director, Medical Information & AI Strategy

Cognito Therapeutics, Inc.; Cambridge (MA); Hybrid; USD 180,000 - 260,000; Full time

Benefits offered by this job

Unlimited PTO

Wellness perks

Virtual medical support

Health, dental, and vision insurance

Job summary

Cognito Therapeutics is seeking an Associate Director/Director of Medical Information to build and lead the MI function from the ground up. This hands‑on role will establish the operating model, technology infrastructure, and SOPs to deliver high‑quality scientific content for Alzheimer’s and neurocognitive diseases.

You will create SRDs, manage medical review workflows, and partner with Regulatory Affairs, Legal, Commercial, and Clinical Development to ensure compliant, accurate content.

Qualifications

• Advanced scientific degree required (PharmD/MD/PhD or equivalent).
• 6+ years of Medical Information experience in device/pharma/biotech.
• Strong writing and communication skills for internal/external audiences.
• Experience building MI capabilities, SOPs, and content libraries.
• Familiarity with FDA/EMA/MDR regulatory requirements.

Responsibilities

• Build the MI function from the ground up, including operating model, tech, and SOPs.
• Develop and maintain the MI quality framework and regulatory alignment.
• Lead medical review processes and establish MRC/PRC with cross‑functional teams.

Skills

Scientific writing

Communication skills

Cross-functional collaboration

Regulatory compliance knowledge

Strategic leadership

Education

PharmD/MD/PhD or equivalent

Tools

Veeva Vault

Salesforce Health Cloud

MedAnswers

Job description

Cognito Therapeutics is seeking an Associate Director/Director of Medical Information to build and lead the MI function from the ground up. This hands‑on role will establish the operating model, technology infrastructure, and SOPs to deliver high‑quality scientific content for Alzheimer’s and neurocognitive diseases.

You will create SRDs, manage medical review workflows, and partner with Regulatory Affairs, Legal, Commercial, and Clinical Development to ensure compliant, accurate content.