Remix Therapeutics

Vice President, Program Team Lead

Watertown, MA · Exec

Sponsorship not specified$293k-$358kDetected 57 days ago

Data EngineeringFDA RegulatoryLeadershipRegulatory Affairs

About the role

develop and present program updates and go/no-go recommendations with clarity and rigor.
Manage the critical path, scenario plans, and risk registry with a bias toward proactive resolution.
Drive lifecycle considerations into the development strategy.
oversee key submissions (IND amendments, briefing documents, NDA/BLA/MAA).
Actively remove roadblocks and problem-solve to drive aggressive timelines by working hands-on with team members to anticipate issues and resolve cross-functional friction.
mentor and develop team members.
Build relationships with clinical thought leaders, patient advocacy communities, and key CRO and academic partners central to REM-422 execution.
Serve as the point person for REM-422 at the Executive Leadership Team (ELT) and Board of Directors; develop and present program updates and go/no-go recommendations with clarity and rigor.
Cultivate strong team morale, a shared sense of mission, and a culture of living Remix's team behaviors; mentor and develop team members.
Strategic clarity. Owns trade-off decisions with confidence and communicates them with precision to Remix's leadership.

Hands-on resource allocation experience against development milestones.
Advanced degree (M.D., Ph.D., Pharm.D., or M.D./Ph.D.) in a relevant scientific or clinical discipline.
Background in oncology drug development with experience in rare solid tumors (ACC, sarcoma, or similar) and/or hematologic malignancies (AML, MDS).
The ideal candidate combines deep development experience with strategic instincts and organizational leadership.
Success in this role is measured by the ability to align diverse perspectives, resolve competing priorities, and move the team forward as one.
Required
Demonstrated PTL or equivalent integrating leadership role on a late-stage asset through pivotal trials and global regulatory submission with direct accountability for cross-functional trade-off decisions.
Preferred
Experience as a Global Franchise Lead or equivalent role with direct commercial exposure: launch planning, label strategy, or market access integration.

15+ years of drug development experience with depth across clinical, regulatory and Tech Ops
experience in oncology strongly preferred.

Remix launched with a vision to transform patients' lives through modulation of RNA processing.
We focus on diseases of high unmet medical need and are committed to operating with scientific rigor and urgency.
Integrate different functional perspectives including clinical, regulatory, CMC, translational, medical affairs, and commercial functions into a single, coherent strategy that maximizes the value REM-422.
Partner with Regulatory Affairs to develop and execute a global regulatory strategy, including FDA, EMA, and other priority health authority engagement

This listing is sourced directly from Remix Therapeutics's careers page and normalized into a canonical job model.