CMC Regulatory Manager

Title: CMC Manager

Location: United Kingdom

Duration: 12-month contract (100% attendance)

Company Overview

Apsida Life Science is currently partnering with a clinical-stage biotechnology company that is developing a potent, selective, and orally bioavailable small-molecule.

Responsibilities

• Support overall CMC program execution for Phase 3 readiness and commercial planning activities
• Develop and maintain integrated CMC timelines, project plans, risk registers, and action trackers
• Coordinate cross-functional meetings with internal stakeholders and external partners
• Track project deliverables and ensure alignment with regulatory and clinical milestones
• Prepare meeting agendas, minutes, and follow-up actions for governance and technical meetings
• Support inspection readiness and due diligence activities as needed
• Budget & Financial Tracking

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