Medical, Legal and Regulatory Facilitator

vor 2 Wochen

Basel, Schweiz Aequor Consulting GmbH Vollzeit

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.

**Benefits**
- 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.

**Job Types**: 100%, Temporary / Staffing
Contract length: 12 months

  • Associate Medical Affairs 100%

    Vor 5 Tagen

    Basel, Schweiz SFL Regulatory Affairs & Scientific Communication Vollzeit

    Would you like to join and contribute to an award-winning, successful and growing multi-national organization in the heart of Europe and one of the world’s leading regions of the pharmaceutical industry? SFL Group and its dynamic cross-functional team provide premium consulting support to companies in the healthcare and life sciences fields. Our clients...

  • Entry Position Medical Writing

    vor 2 Wochen

    Basel, Schweiz SFL Regulatory Affairs & Scientific Communication Vollzeit

    Would you like to join and contribute to an award-winning, successful and growing multi-cultural organization in the heart of Europe and a world-leading region of the pharmaceutical industry? SFL Group and its dynamic cross-functional team provide premium consulting support to companies in the healthcare and life sciences fields. Our clients range from...

  • Director, Regulatory Affairs, Dx/CDx and Medical Devices

    vor 4 Wochen

    Basel, Schweiz BeiGene, Ltd. Vollzeit

    Director, Regulatory Affairs, Dx/CDx and Medical Devices page is loaded## Director, Regulatory Affairs, Dx/CDx and Medical Deviceslocations: Basel: Switzerland Remotetime type: Full timeposted on: Posted Yesterdayjob requisition id: R31506BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When...

  • Director, Regulatory Affairs, Dx/CDx and Medical Devices

    vor 2 Wochen

    Basel, Schweiz BeiGene Vollzeit

    BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. General Description: The Director, Regulatory...

  • Director, Regulatory Affairs, Dx/cdx and Medical Devices

    Vor 3 Tagen

    Basel, Schweiz BeiGene Vollzeit

    General Description: The Director, Regulatory Affairs, Dx/CDx and Medical Devices will be responsible for leading a small team for developing and implementing regulatory diagnostic and medical device strategies as applicable, for the designated program to support clinical trials where necessary, and facilitate marketing authorization in line with business...

  • Regulatory Change Expert

    Vor 3 Tagen

    Basel, Schweiz Julius Baer Vollzeit

    At Julius Baer, we celebrate and value the individual qualities you bring, enabling you to be impactful, to be entrepreneurial, to be empowered, and to create value beyond wealth. Let’s shape the future of wealth management together. Are you an experienced regulatory change expert, which is passionate about the transformation of our industry? In this...

  • Healthcare/pharma Legal Counsel

    vor 2 Wochen

    Basel, Schweiz Axiom Talent Platform Vollzeit

    Take the next step in your career with the leading global alternative legal service provider. Don't compromise. Over twenty years ago, Axiom started a movement to change the face of the legal industry. Today we continue to break boundaries with a combination of top-tier legal talent and globally recognized F500 clients. Trusted by the leading brands around...

  • Global Director of Science and Regulatory

    vor 1 Tag

    Basel, Schweiz Klick Health Vollzeit

    For the past 25 years Klick Health has helped life science clients bring their groundbreaking ideas to market. We’ve also spent that time creating an ecosystem for talented and empathetic individuals to chase their passions while creating long-lasting friendships in the process. What does that mean for you? Well, we grow a lot—like every year for 25...

  • Regulatory Writer

    vor 1 Tag

    Basel, Schweiz Novartis Vollzeit

    500! The number of regulatory documents we authored last year. As a Regulatory Writer you will write and review high quality clinical and safety documentation for submission to regulatory authorities. **Location**: Basel, Switzerland #LI-Hybrid **Your responsibilities**: Your responsibilities include, but are not limited to: - To author and review high...

  • Director Regulatory Affairs, Quality Assurance and

    vor 1 Tag

    Basel, Schweiz BeiGene Vollzeit

    General Description: Under the direction of the General Manager Sub Region Europe, this individual is responsible for the local representation of regulatory affairs and quality assurance in SRE. The incumbent provides dynamic leadership, strategic direction and close oversight of all regulatory affairs and compliance activities in SRE across BeiGene's...