About Us
GCRI is a full-service niche CRO focusing on indications where we have a detailed knowledge and even more important, where we have a strong network.
The indications we focus on are:
Wound Care
- Diabetic Foot
- Leg Ulcers
- Pressure Ulcers
- Acute Wounds
- Atypical Wounds and Rare Disease Wounds
Orthopedic Surgery
- Implants & Prosthetics
- Rehabilitation
- Fractures & Trauma
- Minimally Invasive Surgery
Dermatology
- Chronic Conditions
- Cosmetic Treatments
- Wound Healing
- Inflammatory Disorders
- Topical & Systemic Therapies
Management Team
Bent von Eitzen
CEO
20 years experience in the wound care industry. Leading roles at EWMA, ISDF & ALPS.
Morgan Zelen
COO, (MBA, CCRP)
11 years experience in clinical research directing trial operations at a leading US based CRO.
Mark Cregan
CMO (PhD)
30 years experience in clinical re-search, with 15 years experience in leading clinical trials in academia, followed by 15 years in the medical industry.
Team Members
Joanna James
PhD Clinical Expert
Clinical development and regulatory strategy advisor with expertise spanning the full clinical lifecycle, from designing and planning clinical studies and trials to building global regulatory roadmaps and overseeing all CTA/CTIS submission documentation. Working on post-market activities including PMCF, PMS, and the writing and sign-off of CIRs and CERs are core areas of focus, alongside medical affairs and liaison with PIs, CIs, and KOLs.
Fleur van der Meer
Clinical Trial Assistant
MSc in Pharmaceutical Sciences, with a specialization in Medicine in Society at the University of Copenhagen and a passion for patient wellbeing. Supporting day-to-day trial operations. Assisting in monitoring and data management activities ensuring documentation gaps are resolved and essential study documentation is acquired and logged.
Cristian Thuesen
Clinical Trial Assistant
MSc in Human Physiology with experience in clinical research on COPD patients. Supporting day-to-day trial operations. Assisting in monitoring and data management activities ensuring documentation gaps are resolved and essential study documentation is acquired and logged.
Heidy Gutiérrez
Clinical Trial Manager
Responsible for end-to-end oversight of clinical trials, ensuring compliance with ICH-GCP, CIP, MDR, data integrity, patient safety, and timely study delivery. 6+ years of experience in clinical research, progressing from a strong CRA background with extensive clinical trials experience, with expertise in site management, study execution, protocol adherence, and cross-functional collaboration.
About Us
This focus allows us to offer a premium service to our customers,
With GCRI you always get the A-Team, we do not pull people from your trial to support more lucrative trials, the contact persons for your trial remain the same throughout the trial.
We pride ourselves to be costumer focused and always going that extra mile, to secure the best result.
Let’s Discuss Your Trial Today!
Contact GCRI to learn more about our clinical research services and how we can help you accelerate your innovations.