Medical, Legal and Regulatory Facilitator

Aequor Consulting GmbH; Basel; Vor Ort; CHF 80’000 - 110’000; Vollzeit

Zusammenfassung

A leading life sciences organization seeks a detail-oriented Medical, Legal and Regulatory Facilitator to ensure the smooth operation of MLR processes. This remote role involves managing content review workflows, coordinating stakeholder efforts, and supporting compliance in medical affairs.

Leistungen

Long-term project with global visibility

Opportunity to work with cross-functional teams

Qualifikationen

• Solid experience in MLR facilitation or regulatory content review.
• Familiarity with promotional and non-promotional material workflows.
• Fluent in English, other languages are a plus.

Aufgaben

• Lead digital submission readiness reviews.
• Coordinate with internal and external stakeholders for timely review.
• Track and communicate review status and priorities.

Kenntnisse

Attention to detail

Stakeholder management

Coordination skills

Compliance understanding

Tools

FUSE

Jobbeschreibung

We are seeking a detail-oriented and experienced Medical, Legal and Regulatory Facilitator (m / f / d) to support the global Medical, Legal, and Regulatory content approval process for a leading life sciences organization. The role ensures high-quality execution of MLR processes within the FUSE system for both medical and commercial content.

Your Responsibilities

• Lead digital submission readiness reviews for promotional and non-promotional materials.
• Oversee and manage the entire content approval process across medical, legal, and regulatory (MLR) teams.
• Coordinate with internal and external stakeholders (e.g., project owners, MLR reviewers, agencies, and local affiliates) to route materials for timely and compliant review.
• Conduct readiness checks to ensure that materials are fully prepared for submission.
• Facilitate review and concept meetings, and maintain reviewer task progress and system delegations in FUSE.
• Provide guidance on MLR submission requirements to project owners and vendors.
• Ensure final approved materials are properly documented and marked as “final approved”.
• Track and communicate review status, priorities, and potential delays to all relevant stakeholders.
• Act as both MLR Facilitator and Superuser in the FUSE system, resolving process and system-related issues efficiently.

Your Profile

• Solid experience in MLR facilitation or regulatory content review processes within the pharmaceutical or life sciences sector.
• Familiarity with promotional and non-promotional material approval workflows.
• Experience working with MLR systems, preferably FUSE.
• Strong coordination and stakeholder management skills across cross-functional teams.
• Excellent attention to detail and understanding of compliance requirements.
• Able to work independently in a remote setup and manage multiple priorities under tight timelines.
• Fluent in English (written and spoken); other languages are a plus.
• Remote position.
• Long-term project with global visibility and impact.
• Opportunity to work with cross-functional teams across medical, legal, regulatory, and commercial areas.
• Be part of a high-performance team supporting innovation and compliance in global medical affairs.

Medical Legal And Regulatory Facilitator • Basel, CH