SWEDEN · NORWAY · DENMARK
Clinical Research Services
Across Scandinavia
Operational support for pharmaceutical and medical device clinical studies. From strategic planning through to study start-up and site monitoring, delivered by a senior consultant across all three Scandinavian countries.
We navigate clients through the Nordic clinical research terrain
15+ Years Experience
3 Scandinavian Countries
2 Sectors: Pharma & Medtech
Established 2012
—SERVICES
What We Do
Operational clinical research support across pharmaceuticals and medical devices, from strategic programme oversight to local site-level delivery. Priority services are Clinical Operations, Study Start-Up and Site Monitoring. For other support across clinical development, get in touch.
Clinical Operations
Strategic and operational oversight of clinical programmes. Leading cross-functional teams in the planning and delivery of studies to scope, quality, budget and timelines. Including regulatory market authorisation submissions and lifecycle management.
Study Start-Up
Site identification and feasibility, contract negotiations between sponsors, CROs and clinics, and regulatory and ethics committee submissions across Sweden, Norway and Denmark.
Site Monitoring
Overseeing trial sites to protect participant rights, ensure data integrity and verify protocol compliance on behalf of the sponsor, in accordance with ICH-GCP and applicable regulations.
— WHY NORDIC TRIAL PARTNERS
Built for How Clinical Research Works in Scandinavia
A senior consultancy covering all three countries, both sectors, and moving faster than CROs.
| Senior expertise on every project
Every engagement is led directly by a consultant with 15+ years of operational experience across global clinical programmes.
| Tri-country coverage
One consultancy covering Sweden, Norway and Denmark. No subcontracting between countries, no handoffs, no coordination delays.
| Pharma and medtech
Operational experience across both pharmaceutical and medical device studies. Clinical Operations, study management, study start-up and site monitoring - covered under one roof.
| Fast and reliable
Responsive at every stage, from first brief to final deliverable. Contracts signed and work started within a week if required.
— PROJECT EXAMPLE
Results Across the Nordics
ANONYMISED CASE STUDY
One Partner Across Sweden, Norway and Denmark
An international CRO subcontracted Nordic Trial Partners to run study start-up across all three Nordic countries on a Phase III trial: site contracting, local regulatory guidance and CTIS submissions, handled by one partner instead of six. Sweden, Norway and Denmark became the first three countries in Europe to activate sites and recruit participants. The same pattern repeated across four studies. For the one study run by a different supplier, none of the Nordic countries recruited early.
3 countries, one partner
Top 3 in Europe to activate and recruit
4 studies, Nordics first each time
David was the fourth Director of Global Clinical Operations assigned to our programme-critical Phase II trial, and the one who stayed until close-out. He held the CRO to its agreement, renegotiated the budget with million-dollar savings, and against all odds we completed the trial to the quality, budget and timelines the project team had agreed.
Katarzyna Piskulak, Global Study Manager
International pharmaceutical company
— ABOUT NORDIC TRIAL PARTNERS
David Antonsson
Senior clinical research consultant with 15+ years of global experience across pharmaceuticals and medical devices. Founded in 2012, based in Gothenburg, operating across Sweden, Norway and Denmark.
Need Clinical Research Support?
Get in touch to discuss your project. Typically responds within 24 hours.