argenx is a fast-growing clinical-stage biopharmaceutical company developing innovative potential therapies to help improve the lives of people suffering from severe autoimmune diseases. Our global team is committed to living by our values of collaboration, empowerment, humility, innovation and excellence. As we continue to expand our therapeutic franchises, spanning neuromuscular, hematology, dermatology and nephrology, we remain science-based, data-driven and patient-focused.
To support the growth of our Translational Science biomarker team, argenx is seeking a highly motivated biomarker associate scientist with a strong background in immunology research. In this pivotal role, the biomarker associate scientist will support the implementation of biomarker assays, collaborating closely with both internal and external project teams. We are specifically looking for a versatile scientist who is eager to engage in various projects and possesses expertise in the development, analytical validation, and outsourcing of clinically relevant biomarker assays. Hands-on experience with ligand binding assays, along with excellent communication skills, will be highly valued.
This role is based in Zwijnaarde (Ghent).

Main roles & responsibilities

• Act as a biomarker study monitor, supporting the implementation of biomarker assays, including assay development and validation, as well as biomarker sample analysis, both internally and/or in collaboration with external vendors or academic collaborators
• Serve as a subject matter expert in ligand binding assays, providing support across multiple programs and ensuring the adherence to best practices
• Review of method validation and sample analysis plans and reports
• Review and provide input in clinical trial related documents (protocol, data transfer agreement, lab manual…)
• Initiates and follows up on troubleshooting of biomarker methods
• Presenting results and findings at internal multidisciplinary project/clinical teams
• Contribute to the growth and further development of the Translational Science team

Professional experience / expertise:

• Master degree in Immunology, Life Sciences or Molecular Biology with at least 5 years of relevant research / industry experience, or Bachelor degree with minimum 7 years of industry experience in analyzing human samples and/or monitoring analysis of biomarkers during clinical trials
• Good knowledge of bioanalytical techniques specifically in the field of biologics and antibodies
• Solid knowledge in the development and validation of ligand binding assays
• Hands-on experience with ligand-binding bioanalytical methods on ELISA, MSD or Gyrolab is considered an asset
• Experience in managing outsourced activities at external Contract Research Organizations (CROs) is considered an asset
• Understanding of GCP/GCLP guidelines and current global regulations is an asset

Profile:

• Team player, motivated, enthusiastic, accurate in execution and reporting
• Strong organization, and interpersonal skills
• Good communication skills and good written and oral English language skills
• Team-player, capable to collaborate effectively with internal and external stakeholders

Offer:

• Full time position in a collegial, dynamic and growing company
• Work in a cross-functional team with access a broad array of technologies
• Opportunity to contribute to the continued build out of the Translational Science team
• Exposure to all aspects of nonclinical and clinical development in the company, but also with external vendors, contract partners and the scientific world
• A competitive salary package with extensive benefits
• A work environment in a human-sized, dynamic, rapidly growing biotech company
• Open to hybrid work with multiple days a week spent working in the Zwijnaarde (Ghent) office

LI-onsit

• Act as a biomarker study monitor, supporting the implementation of biomarker assays, including assay development and validation, as well as biomarker sample analysis, both internally and/or in collaboration with external vendors or academic collaborators
• Serve as a subject matter expert in ligand binding assays, providing support across multiple programs and ensuring the adherence to best practices
• Review of method validation and sample analysis plans and reports
• Review and provide input in clinical trial related documents (protocol, data transfer agreement, lab manual…)
• Initiates and follows up on troubleshooting of biomarker methods
• Presenting results and findings at internal multidisciplinary project/clinical teams
• Contribute to the growth and further development of the Translational Science tea