(Senior) Associate Scientist in vivo
(Senior) Associate Scientist in vivo
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Job Description
Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets led by VYVGART our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG and with the potential to treat patients across dozens of severe autoimmune diseases.
We are building a new kind of biotech company one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company our partnerships our science and our people because when we do we deliver more for patients.
We are seeking a highly motivated pro-active and skilled in vivo (senior) associate scientist to join our team. You will be responsible for conducting coordinating and overseeing in vivo studies and sample analysis to support project teams. This includes ensuring compliance with ethical guidelines and contributing technical and scientific input on study design execution and analysis. You will also act as the primary liaison for outsourced in vivo studies managing communication coordination and stakeholder relationship with external collaborators.
The job is based in our facility in Zwijnaarde Belgium. Daily presence on site is expected.
Note that a motivation letter must be included with your CV. Only candidates who submit a genuine motivation for this in vivo role will be considered.
Work description
Experimental support
- Perform hands-on in vivo procedures including mouse handling IV/IP/SC injections and blood sampling.
- Support sample analysis workflows; experience with ELISA and MSD platforms is a plus.
- Provide technical and scientific input on study design execution and data interpretation by actively engaging in project teams.
Operational oversight & coordination
- Act as main point of contact for in vivo workflow both internally as well as with external partners.
- Support and coordinate study planning logistics and stakeholder alignment for internal and outsourced studies.
- Maintain up-to-date documentation and ensure compliance with institutional and ethical guidelines including drafting and managing ethical dossiers and protocols.
- Continuously seek opportunities to improve internal workflows and support project teams.
Profile
- A Master degree in Biomedical Sciences Biochemistry Biotechnology or equivalent with at least 4 years of relevant experience.
- FELASA C certification (or equivalent) required.
- Proven experience with in vivo techniques such as mouse handling IV/IP/SC injections and blood sampling.
- Knowledge and hands-on experience with ELISA and MSD platforms.
- Strong organizational and communication skills with fluency in English (written and spoken).
- Ability to work independently and collaboratively in a fast-paced cross-functional environment.
- A pro-active solution oriented mindset with a passion for scientific excellence.
Offer
- A full time position in a successful dynamic rapidly growing biotech company.
- A competitive salary package accompanied by comprehensive benefits.
- Joining a team that provides access to a wide range of technologies engaging in diverse daily tasks and encouraging initiative-taking to contribute to the companys success.
#LI-Onsite
At argenx all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race color religion sex sexual orientation gender identity national origin protected veteran status disability or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.
Before you submit your application CV or any other personal details to us please review our argenx Privacy Notice for Job Applicants to learn more about how argenx B.V. and its affiliates (argenx) will handle and protect your personal data. If you have any questions or you wish to exercise your privacy rights please contact our Global Privacy Office by email at .
Required Experience:
IC
Employment Type
Full-Time
