Clinical Trial Manager

Do you dare to shake up the medical world and improve the lives of patients with chronic degenerative diseases?

Allegro is a revolutionary start-up that designs and develops ground-breaking biomedical nanotechnology for the treatment of osteoarthritis. We are hiring you as

Clinical Trial Manager

The Job

We are seeking a hands-on scientist with a passion for life sciences to join our team as a Clinical Trial Manager. As a Clinical Trial Manager, you work directly with the CSO and QM of the company. You will actively participate in research projects and production jobs. You like to work hands on in the lab, as well as do desk research.


  • Develop and implement comprehensive clinical trial protocols in compliance with regulatory requirements and company standards.
  • Oversee all aspects of clinical trial operations, including site selection, investigator meetings, and monitoring activities to ensure adherence to protocol and timelines.
  • Coordinate with cross-functional teams, including medical affairs, regulatory affairs, and research and development, to facilitate the execution of clinical trials.
  • Manage budget and resources effectively, ensuring optimal allocation to meet project objectives within financial constraints.
  • Lead study meetings and provide guidance to study team members and investigators on trial-related activities and processes.
  • Establish and maintain relationships with key stakeholders, including clinical investigators, study coordinators, and CROs, to foster collaboration and ensure smooth conduct of trials.
  • Monitor and report on trial progress, identifying and addressing issues or risks that may impact study timelines or data integrity.
  • Ensure compliance with Good Clinical Practice (GCP) guidelines, regulatory requirements, and internal SOPs throughout the conduct of clinical trials.


  • Minimum of 5 years of experience in clinical trial management, preferably in the medical device industry and/or within the field of osteoarthritis.
  • In-depth knowledge of clinical trial regulations, including FDA and MDR guidelines, and experience with regulatory submissions and audits.
  • Strong project management skills with the ability to effectively prioritize tasks and manage multiple projects simultaneously.
  • Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal and external stakeholders.
  • Proven leadership abilities, including the ability to lead cross-functional teams and motivate team members to achieve project goals.
  • Detail-oriented with strong analytical and problem-solving skills, capable of identifying and resolving issues in a timely manner.
  • Proficiency in Microsoft Office Suite and experience with clinical trial management systems (CTMS) and electronic data capture (EDC) platforms.

Your Profile

You have a:

  • Master’s degree in biomedical sciences, medicine, or similar.
  • English CEFR C2 (Mastery level)
  • Experience in a similar role is a plus but not mandatory.

You have the following skills:

  • Science-driven, business-focused: applying state-of-the-art innovation to achieve strategic goals within a business context.
  • Analytical Skills: Demonstrate strong analytical and problem-solving abilities, with the capacity to leverage data and insights to drive informed decisions.
  • Planning and organization: work in a very well-structured manner
  • Meticulous perfection meets operational performance: a uniqe ability to deliver the highest quality work in short timelines.
  • Communication and Relationship Building: Exhibit excellent communication skills, both verbal and written.
  • Strategic Thinking: Display a strategic mindset and the ability to envision long-term goals while effectively managing day-to-day operations. Stay updated on industry trends and best practices to drive innovation.

Our offering

As a company

An impact- and purposeful environment, in a young start-up that can change the lives of many people suffering from osteoarthritis.

A high-performance and eager culture, An easy and uncomplicated team, but very eager and high-performance.

An opportunity to learn a lot, and grow together with the company, make a positive impact, and build tomorrow’s future. The job allows for an ambitious person to build a great career as a top executive.

For you

  • A great remuneration package with a substantial salary.
  • Company car.
  • Extra-legal benefits (hospitalization insurance, meal vouchers, …)
  • Premium working tools.

You are stationed in our Liège research laboratories.


Do you want to join the future? Contact us via e-mail: