Lundbeck
- Location:
- Copenhagen, Zealand, Denmark
- Salary:
- Competitive
- Type:
- Permanent
- Main Industry:
- Search Manufacturing Jobs
- Advertiser:
- Lundbeck
- Job ID:
- 131198453
- Posted On:
- 05 October 2024
Clinical Biomarkers Specialist
Do you have a strong technical acumen with in-depth experience in developing and validate biomarker assays to be implemented in clinical trials? Is working in a cross-functional environment, supporting clinical trials and to shape the future of clinical biomarkers something you are looking for? Then, this opportunity is for you!
Your new role
-As a Fluid Clinical Biomarker Specialist, you will lead the development and validation of assays in a regulatory environment, working closely with internal stakeholders to ensure effective project execution.
-Work closely with biomarker lead to align on assay requirements and be the point of contact when interacting with CROs to coordinate proposals, work orders, support bioanalytical processes etc.
-Provide technical and strategic input to programs as needed.
-Represent Lundbeck when interacting with CROs, attending conferences etc., and conducting site audits.
-You will have the opportunity to evaluate and bring in new technologies as needed.
Your future team
The Clinical Biomarkers team is lead by the Head of Clinical Biomarkers whom you will report directly to. We are 7 team members with expertise in both fluid and imaging biomarkers and collaborates across our specialties supporting clinical trials as well as with our colleagues in Research. The Clinical Biomarkers Department is part of Experimental Medicine within Global Clinical Development at Lundbeck.
The position is based in Valby, Denmark.
What you bring to the team
To learn and thrive in this role, you should have:
-A MS +10 years or PhD +4 years of experience in a similar role from pharma, biotech or CRO.
-Expertise in developing, validating, and troubleshooting bioanalytical methods for both large and small molecules, using a variety of analytical techniques such as immunoassays, genotyping, RNAseq and LCMS methods.
-Experience in outsourcing and supervising assay development and bioanalysis of small molecules and biologics to CROs as well as some bioanalytical operational experience.
-Evidence of working knowledge of regulatory requirements, including experience with GLP/GCP, and applying these regulations when writing study plans and reports.
-Collaborative mindset and skilled in interpersonal interactions and stakeholder management.
-Proficient in spoken and written English.
Our promise to you
Lundbeck offers an inspiring workplace and innovative culture, where our curiosity, accountability and adaptability enable us to transform lives. We want to go faster and further on addressing the big unmet needs of people living with brain disorders. We offer rewarding careers with a mix of exciting tasks and development opportunities that are balanced with initiatives focused on your well-being.
We need every brain in the game, and at Lundbeck, we are committed to building a workforce that is as diverse as the people we serve. Read more about our commitment at lundbeck/global/about-us/our-commitment/diversity-and-inclusion.
Apply now
Can you see yourself in this role? We want to hear from you. Does this sound like your dream job, but you’re not sure if you meet all the requirements? We still want to hear from you!
Upload your CV and include a few lines about your motivation for applying. We ask you not to include a photo or personal information that does not relate to your professional experience.
Applications must be received by 29 October, 2024.
Learn more about us at lundbeck, LinkedIn or Instagram (h_lundbeck).
#EveryBrainInTheGame
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