Are you good at paying attention to details and currently enrolled in an academic program studying Life Sciences or equivalent, now is your time to join our Global Regulatory Affairs team as our new student assistant.

Ascendis Pharma is a fast-growing biopharmaceutical company with locations in Denmark, Germany, the United States, UK, Italy, Spain, and France.
We are applying our Trans Con® technology to build a leading, fully integrated biopharmaceutical company focused on making a meaningful difference in patients’ lives. Guided by our core values of Patients, Science, and Passion, we use our Trans Con® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.

We are seeking a curious and organized Student Assistant to join our Global Regulatory Affairs (RA) Function. As a Student Assistant in Global RA, you will work with your regulatory colleagues across departments in DK and in US, and be involved in a variety of tasks, both general department assistance and document handling and archiving tasks. You will become part of a global team with a large network, and it will be a great opportunity for you to grow professionally and get your foot in the door to a great biotech company.
You will be based in Hellerup and report directly to Pernille Skindhøj, Senior Director Device Regulatory Affairs.
As a Student Assistant you will have a variety of supporting tasks and be working in different IT systems, in particular our document handling system (Veeva). We will provide the needed training and mentoring to get you started and continuously add more to your skills

Furthermore, your tasks will be:

• Archiving of documents and correspondences across projects
• Archiving of Health Authority Questions in our database
• Assign training, and upload content in our Learning Management System:
• Support the Regulatory Strategy team and Regulatory Operation with proof reading / QC check of documents before submission
• Support Product Variations with document handling
• Support internal process and administrative tasks across the regulatory function.

Qualifications and skills:
You are currently enrolled in an academic program studying Life Sciences or equivalent. Preferably, you are in your second or third year of your study.

Furthermore, you have:

• The ability to keep an overview of many tasks at the same time
• Structured with a strong focus on details
• Strong communication skills
• Excellent English skills, especially written
• Interest in working in different IT systems
• Interest in regulatory affairs

Work hours: 15 hours per week. You can expect up to 20 hours per week during peak periods. During exam periods, we offer flexibility where possible to help you balance your studies and work responsibilities.
Office: Ascendis Pharma A/S (Headquarter), Tuborg Boulevard 12, Hellerup, Denmark

For more details about the position or the company, please contact Pernille Skindhøj, Senior Director Device Regulatory Affairs, pls@asceendispharma.com or visit our website Ascendis Pharma

All applications must be submitted in English and are treated confidentially.

Applications will be evaluated when received, so please apply as soon as possible.