Chief Scientific Officer

About The Job

RedFox Therapeutics is an emerging biotech dedicated to developing first-in-class drugs for underserved diseases. Our lead pipeline candidate is a preclinical-stage small molecule, for an orphan cornea condition without any FDA-approved therapies.

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Role Overview

We are seeking an exceptional Fractional Chief Scientific Officer to provide strategic scientific leadership during our formative stages. This role offers a unique opportunity to shape RedFox’s scientific vision and research strategy

The ideal candidate will bring deep expertise in ophthalmology drug development, proven leadership in biotech environments, and the ability to translate complex science into compelling business narratives for investors and partners.

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Key Responsibilities

Scientific Strategy & Leadership:

• Lead RedFox’s overall development strategy for a first-in-class candidate for an orphan cornea disease
• Provide strategic oversight of preclinical development and IND-enabling studies
• Lead data interpretation and scientific decision-making processes

Clinical Development Oversight:

• Coordinate with CROs to oversee a robust preclinical development program
• Lead safety and efficacy studies to support regulatory submissions
• Support preparation of regulatory documentation including IND submissions and FDA interactions

Stakeholder Engagement & Communications:

• Serve as scientific spokesperson to investors, partners, and key opinion leaders
• Engage with external scientific advisory boards and key opinion leaders in ophthalmology
• Represent the company at scientific and industry conferences

Team Development & Operations:

• Support recruitment and development of additional scientific talent as the organization grows

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Required Qualifications

Education & Experience:

• PhD in relevant life sciences discipline (biochemistry, cell biology, chemistry or related field)
• 10+ years of progressive experience in pharmaceutical or biotechnology R&D, with significant leadership responsibilities. Preferably with direct experience with cornea diseases.
• Proven track record leading preclinical development programs from discovery through IND submission

Technical Expertise:

• Strong understanding of regulatory requirements for ophthalmology drug development, including FDA guidance documents

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What We Offer

Compensation & Equity

• Competitive fractional compensation commensurate with experience
• Meaningful equity package for milestones met, with potential for significant upside as the company grows
• Flexible fee structure options including hourly or monthly retainer arrangements

Work Environment & Flexibility

• 100% remote work with flexible scheduling around your existing commitments

Commitment & Timeline

• Expected time commitment: 10-20 hours per week, with flexibility to adjust based on company needs and development milestones
• Initial engagement: 12–24 month term with potential for extension or conversion to full-time role

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How to Apply

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