Global Medical Lead

Scorpion Therapeutics; United States; Remote; USD 180,000 - 260,000; Full time

Job summary

Outlook Therapeutics seeks a Medical Affairs Lead to oversee medical and scientific aspects during the US and global launch of an FDA-approved ophthalmic treatment for wet AMD. You will guide clinical practice patterns, supervise medical review of materials, and drive evidence generation strategies including real-world evidence and investigator-initiated studies.

You will build training for cross-functional teams, engage KOLs, and support market access and launch activities, collaborating with

Qualifications

• MD, PharmD, or PhD with 10+ years in Medical Affairs, Clinical, or related fields, with deep expertise in retina and evidence-generation models, and experience in medical review and sign-off.

Responsibilities

• Provide medical and scientific oversight during US and global launch.
• Guide medical governance and ensure compliance of promotional and scientific materials.
• Drive evidence generation strategies including RWE and investigator-initiated research.
• Build training programs for cross-functional teams and engage with external KOLs.

Skills

Medical affairs leadership

Retina expertise

Medical review & sign-off

Evidence generation

Cross-functional collaboration

Education

MD/PhD/PharmD

Job description

Role

Medical Affairs Lead for Outlook Therapeutics, responsible for medical and scientific oversight during US and global launch of an FDA-approved ophthalmic treatment for wet AMD. Responsibilities include providing clinical and scientific guidance on practice patterns, managing medical review and sign-off of promotional and scientific materials, driving evidence generation strategies (including RWE and investigator-initiated research), and ensuring medical governance and compliance. The role involves building training programs for cross-functional teams, engaging with external KOLs, guiding scientific communication, and supporting market access and launch activities. Collaboration with senior leadership, clinical, regulatory, commercial, and market access teams.

Requirements

• MD, PharmD, or PhD with 10+ years in Medical Affairs, Clinical, or related fields, with deep expertise in retina and evidence-generation models, and experience in medical review and sign-off.

Preferred

• active medical licensure
• board certification (retina/ophthalmology)
• global market experience
• familiarity with pharmacovigilance

High-value

• ophthalmology, retina, wet AMD, evidence-generation, regulatory and compliance oversight, global scope, remote US-based with international interaction.