About Us

Vertanical – A World Free of Chronic Pain. We are a leading global biopharmaceutical company specializing in the development and distribution of innovative medicines for the treatment of chronic pain. Our vision is clear: a world free of chronic pain! With VER-01, we have developed a unique cannabinoid-based medicine for the treatment of chronic pain, which was approved in Germany and Austria in June 2026 under the name Exilby. This marks a significant milestone after more than eight years of intensive research and development.

Approval in the USA is planned for 2029. Our goal is to establish Exilby as the leading therapy for the treatment of chronic pain by 2030, setting new standards in pain management. Does

this sound exciting to you? Then apply now! We look forward to getting to know you.

Your mission with us

Shape the future of pain therapy with us! In this role, you will ensure the highest quality standards in our clinical trials. You will actively contribute to our Clinical Quality Assurance System, identify risks early, and ensure compliance with regulatory requirements. Working closely with internal teams and external partners, you will drive improvements and ensure consistent quality implementation. Ready to take on responsibility and make a real difference? Then we're looking for you!

Your tasks

You are responsible for the design, maintenance, and improvement of our CQA system.
Your focus is on the identification, documentation, evaluation, and follow-up of protocol deviations and non-compliances at study centers.
You identify trends early on in order to take preventative measures.
You are responsible for coordinating with external service providers (e.g., monitoring CROs) to prevent and correct non-compliance through the development of CAPA measures.
You will act as a sparring partner to our Clinical Operations Team regarding all center-related GCP topics.

Your profile

You have a completed degree in medicine, natural sciences, pharmacy, biotechnology or a similar field.
You have at least 1 year of prior experience in clinical research and quality assurance and ideally have already gained experience as a CRA.
You already have an in-depth understanding of ICH GCP E6 and related regulations.
You have experience in designing and improving business processes.
You work independently, in a results-oriented and structured manner.

How To Apply:

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Responsibilities