Clinical Trial Specialist

Byondis is an independent Dutch biopharmaceutical company, based in Nijmegen, that focuses on developing innovative medicines against cancer and autoimmune diseases. We are driven by one goal: to develop new treatments to improve the standard of care for patients.

Your role
As a Clinical Trial Specialist, you will be working on Clinical Development trials initiated by Byondis and provide support to the Clinical Trial Teams and Clinical Project Leaders. Byondis outsources most of the operational aspects of its clinical trials to contract research organizations (CROs) and internal and external contract laboratories and as such you will often work together with CRO/lab personnel.

• You are involved in the many different logistical and operational activities in conjunction with the operational set-up and execution of the clinical trials including vendor management, review and reconciliation of clinical data and laboratory data, financial forecasting and oversight, archiving and general Sponsor oversight of clinical trial activities.
• You assist in, or are responsible for, preparing different types of documents and systems used in the preparation and execution of clinical trials.
• You also assist in the planning, organization and execution of investigator, expert and other types of meetings.
• It is expected that you quickly work independently on more than one project in parallel and have an intuitive feel for optimal organization and logistics for your projects.
• You enjoy working in a cutting-edge research environment and a fast-paced clinical and product development organization.
• You work within a team of approximately 10 Clinical Development professionals and will report to the Senior Director Clinical Development.

Your profile and skills
When considering candidates, we are looking for clinical trial professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

• Master’s degree in life sciences.
• A minimum of 3 years relevant experience within clinical operational disciplines in the pharmaceutical industry, a commercial or university clinical research organization, or equivalent experience (such as Regulatory Affairs, Medical Information etc.).
• Excellent verbal and written communication skills in English.
• Knowledge of drug development (ICH GCP) regulations.
• Project-management skills and experience.
• Excellent attention to detail and initiative.
• Scientific/clinical or analytical knowledge base, with ability to assess, aggregate, analyze and report data.
• Able to work within a team, liaising efficiently with internal departments and third parties.
• Ability to manage a high workload and the pressure of deadlines.

What we offer you

Benefits and well being
Besides a competitive salary, we offer you a dynamic working environment at our state-of-the-art campus in Nijmegen.  Our values as integrity, authenticity, entrepreneurship, quality and trust are very highly regarded. We also offer a good pension scheme, 30 days annual holidays based on a full-time position and we organize several company events throughout the year.

Join Byondis and create the future you want, today
Contract hours: 32-40 hrs./week, preferably full-time
Salary: depending on experience
Location: Nijmegen

Applicants must be nationals of a Member State of the European Union or hold a valid work permit for the European Union.

For further information, please contact Human Resources, at tel. +31 (0)24 679 5100 or by email; recruitment@byondis.com. If you are interested in joining Byondis in this challenging position, we welcome your application via the apply button. Please send your application before January 6 ^th , 2025.

Acquisition by any commercial agencies will not be appreciated.