Clinical Project Manager

Location: Netherlands (preferable), Denmark, UK or Austria.

This role is only open to candidates that already have the right to work in the EU. No sponsorship available.

The Company

We are partnered with a rapidly growing, emerging clinical stage Biotech headquartered in the Netherlands. They are poised to make a significant impact within the field of blood disorders. Led by the Chief Medical Officer, and Head of ClinOps, this small company are looking to make remarkable strides in the development of groundbreaking clinical studies.

The Role

As Clinical Project Manager you will play a pivotal role in the successful execution of our clinical studies. You will have the opportunity to work on a wide range of tasks, from the nitty-gritty details like routing CDAs for countersignature and document filing to the more strategic responsibilities such as selecting providers, approving proposals, managing budgets, and setting up procedures for study execution.

Main Responsibilities

• Lead clinical studies (Phases I-III) and manage vendor selection and coordination.
• Oversee core document management and handle regulatory submissions and contract budgets.
• Demonstrate a deep understanding of the scientific aspects of the study and efficiently organise meetings.
• Maintain meticulous oversight and control of all study elements, including investigational product (IP) management and quality assurance.
• Display strong leadership and ownership, foster intensive cooperation with various teams, and ensure effective communication while contributing to Standard Operating Procedures (SOPs).

Requirements

• Advanced education in natural sciences or medicine
• Minimum 5 years of relevant industry experience
• Proven track record in clinical trial management
• Up to 25% travel
• Strong communication skills
• Excellent team player

How to Apply

Apply here for a confidential call about this opportunity.