Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.
This role is an exciting opportunity to contribute to a dynamic, ambitious team in Regulatory. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.
Main Responsibilities:
- Support feasibility assessments for new clinical studies, including country feasibility confirmation and mapping activities across Northern Europe
- Evaluate healthcare systems, hospitals and standards of care to inform study planning
- Provide local medical expert input into study design and support study operationalization
- Resolve protocol-related medical and scientific questions from sites and support study teams
- Engage with HCPs, investigators and contribute to patient panels and interviews
- Deliver medical and scientific trainings on disease, compound and protocol to relevant teams
- Provide medical support during investigator meetings and across study activities
- Contribute to cross-country clinical study execution across Nordics, Baltics, Netherlands and Belgium, including setting diversity targets where applicable
Requirements
- Advanced degree (MD, PharmD, PhD in life sciences or equivalent)
- Strong scientific and medical background
- Knowledge of ICH, GCP and local regulations
- Neurology and/or Dermatology experience preferred
- Fluent in English
- Strong stakeholder management skills
- Strong communication and analytical capabilities
- Ability to navigate matrix organizations
Benefits
At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.
Here's what makes us unique.
We are a young, ambitious health company representing 900 Excelyates, driven to become Europe's leading mid-size CRO with the best employee experience. Our one-stop provider service model offering full-service, functional service provider, and consulting enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.
Excelling with care means benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.
Other open roles at Excelya(6)
Excelya is an independent, Paris-headquartered contract research organization (CRO) founded in 2014 that supports biotech, pharmaceutical, and medical device companies with full-service CRO, FSP, and resourcing solutions across clinical development. The company operates through a global network with 900+ experts and coverage in 25 countries, offering capabilities in areas such as clinical operations, data management, biometrics, pharmacovigilance, regulatory affairs, and medical affairs to help clients deliver clinical trials and bring new therapies to patients.
Key team members

Julien Sallaind

Elitza Ouzounova

Emilie Stefanelli

Laurence MAUNIER
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