Global Change Facilitator – Regulatory CMC

This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• Oversee and manage a portfolio of Regulatory CMC workstreams.

• Foster dynamic and collaborative settings that promote participation, knowledge-sharing, and alignment within the industry.

• Steer workstreams by employing structured project and change management methodologies to achieve designated objectives within established timelines.

• Organize and facilitate both virtual and face-to-face meetings, workshops, and events for senior industry leaders.

• Collaborate in the creation of impactful deliverables such as industry guidance, position papers, best practice frameworks, proof-of-concept studies, and conference materials.

• Track member engagement and proactively address risks or obstacles to advancement.

• Enhance and maintain internal systems, reporting tools, and collaborative platforms.

• Document and communicate value narratives that showcase the benefits of industry collaboration.

• Relay member insights back to the organization to facilitate ongoing improvement and future Phorum development.

⛳️ Requirements

• Bachelor’s degree or equivalent experience in life sciences, pharmaceuticals, biotechnology, regulatory affairs, or similar fields.

• In-depth knowledge of Regulatory CMC in the biopharmaceutical sector.

• Experience in pharmaceutical, biotechnology, CDMO, consulting, or regulatory settings.

• Demonstrated experience in managing projects, initiatives, or change programs.

• Strong skills in facilitation and stakeholder management.

• Ability to distill complex technical and regulatory information into clear, actionable insights.

• Excellent organizational abilities to handle multiple priorities and meet deadlines.

• Comfortable working in fast-paced, evolving environments.

• Confident in remote work and collaboration with global teams and diverse cultures.

🏝️ Benefits

• Flexible working environment.

• International exposure.