Elisabeth brings over a decade of experience to her role as Project Manager at CLINIGMA®. Her cross-sector expertise, including work at Novo Nordisk and L’Oréal, is matched by a strong quality mindset and project execution skills critical to successful in-trial interview delivery.

Project Leadership in Clinical Research

• Manages qualitative patient interview projects for pharmaceutical clients across therapeutic areas
• Develops and oversees project proposals and study timelines aligned with trial protocols and GCP standards

Stakeholder and Client Engagement

• Skilled in cross-functional coordination involving internal teams, sponsors, CROs, and site staff
• Communicates project milestones and timelines with clarity and consistency
• Brings commercial and supply-side understanding to project scoping and feasibility

Pharmaceutical Industry Knowledge

• Former consultant in the life sciences sector with experience in GMP/GDP, validation, and quality processes
• Deep familiarity with pharmaceutical workflows from planning to production
• Past experience with regulatory, QA, and clinical supply functions within global companies

Education and Professional Development

• MSc in Supply Chain Management, Copenhagen Business School
• BSc in Economics and Business Administration
• Exchange semester in Project Management and Intercultural Business at Peking University
• Currently undertaking professional certification in project management (Mannaz)

Elisabeth’s structured approach, collaborative mindset, and depth of experience in regulated healthcare industries make her a strong asset to CLINIGMA®’s project delivery team. Her ability to manage operational complexity while prioritising patient experience ensures smooth execution of in-trial interview studies at every stage.