Senior Director, Medical Information

Scorpion Therapeutics; United States; Remote; USD 180,000 - 240,000; Full time

Job summary

Immatics is seeking a Senior Director, Medical Information to lead the MI function in support of cancer immunotherapy programs. You will shape strategy, governance, and content development across SRLs, FAQs, and evidence dossiers while ensuring US MI regulatory compliance.

This is a fully remote role within the US with occasional travel (10–20%). You will partner with Medical Affairs, Regulatory, Clinical, and Market Access to drive MI metrics and enable successful product launches.

Qualifications

• Bachelor's in life sciences required.
• 15+ years in pharma/biotech with Medical Information and Medical Affairs experience.
• Advanced degree (PharmD, PhD, MD) preferred.

Responsibilities

• Lead MI strategy, governance, and content development (SRLs, FAQs, evidence dossiers).
• Oversee call center readiness, onboarding, training, quality oversight, and escalation processes.
• Support payer guidelines and evidence submissions.
• Collaborate with Medical Affairs, Regulatory, Clinical, and Market Access teams.
• Develop MI metrics and insights; build organizational capabilities.

Skills

MI leadership

Strategy development

Vendor management

Cross-functional collaboration

Regulatory compliance

Education

Bachelor's in life sciences

PharmD/MD/PhD preferred

Job description

Role:

Senior Director, Medical Information at Immatics, overseeing the development and leadership of the Medical Information (MI) function to support product launch and pipeline expansion in cancer immunotherapy, specifically targeting PRAME across multiple modalities.

Responsibilities:

establish MI strategy, infrastructure, governance, and vendor partnerships; manage call center readiness, including onboarding, training, quality oversight, and escalation processes; lead scientific content development, including SRLs, FAQs, and evidence dossiers; support payer guidelines and evidence submissions; collaborate cross-functionally with Medical Affairs, Regulatory, Clinical, and Market Access teams; develop MI metrics and insights; and build organizational capabilities.

Requirements:

Bachelor's in life sciences; 15+ years in pharma or biotech with significant MI and Medical Affairs experience; advanced degree (PharmD, PhD, MD) preferred; oncology and cell therapy experience highly desirable; expertise supporting product launches, developing MI content, managing vendors, and ensuring compliance with US MI regulations.

High-Value:

focus on oncology, cell therapy, PRAME target, early-stage or pipeline products, US market, and AI-enabled tools.

Work Setup:

Fully remote within the US with approximately 10–20% travel for congresses, vendor meetings, and internal collaborations.