STUDENT ASSISTANT – CLINICAL OPERATIONS

Are you interested in clinical trials – and eager to learn how they are managed in an international setting?
Do you have flair for quality and are eager to take on responsibility? Then, keep reading - we are looking for a proactive and self-motivated student assistant for Clinical Operations at our head office in Valby.

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. No separate cover letter is needed. We ask you not to include a photo or personal information that does not relate to your professional experience.
If you have questions or want to hear more, please feel free to contact Pernille Strandfelt, Manager, Clinical Operations, phone +45 3083 2815.
Applications must be received by September 10th, 2025.
Learn more about us at www.lundbeck.com, LinkedIn or Instagram (@h_lundbeck).

EveryBrainInTheGame

This job ad is intended for individuals seeking a career opportunity with Lundbeck. We engage with recruitment and search firms where needed on the basis of a written agreement, and we do not accept unsolicited requests of any kind. If you work as a recruitment consultant, you are kindly instructed to refrain from contacting Lundbeck or the hiring manager directly with suggested candidates. If you violate this policy, you do so at your own risk and for your own account, and Lundbeck will not assume any liability nor pay any associated fees resulting from such violation.

As part of our team of 5-7 student assistants, you can expect to collaborate closely with Clinical Operations to handle key task within compliance, quality and administrative support. You will work both independently and collaboratively within the team, and you will gain knowledge and insights to the daily operations in a large complex pharma organisation.
We’re also interested in hearing your suggestions, and this is a great chance to start your career in a role that offers a high degree of collaboration and many learning opportunities.

In your new role, you will:

• Perform quality controls of various clinical documentation and ensure archiving in our electronic systems
• Handling contracts – including electronic signature collection and archiving
• Book flight tickets and process expense reports
• Various general ad hoc tasks supporting our department and trial managers

You can expect to work a maximum of 12-16 hrs per week. Your work hours are flexible and can be adjusted to match your classes and exam periods.