Experienced Safety Surveillance Advisor

afety Surveillance is a department within Global Pharmacovigilance & Clinical Development, and we are a team of enthusiastic and skilled professionals that has global responsibility for surveillance activities. You will be responsible for monitoring the benefit-risk profile of ALK’s products and representing safety surveillance in clinical development projects and post-marketing activities. You will be performing critical safety data analysis and writing aggregated safety reports as well as evaluating the product safety profile.

Your tasks include:

• performing signal detection and analyse large datasets.
• write aggregated safety reports.
• perform scientific review of individual case reports.
• represent Safety Surveillance in cross-functional teams.
• contribute to development of clinical study protocols.
• chair and participate in cross-functional groups.
• communicate benefit-risk assessments to health authorities.
• communicate with external parties.

You will work independently and in collaboration with the highly skilled safety surveillance team and other colleagues across the functional areas in Research & Development at ALK. Oure set up allows for great variety in daily tasks and interactions with many stakeholders across the company. It is a role with significant responsibility, allowing for the opportunity to develop, contribute and make an impact.

What you bring
To be a success in this role, you have a background in medical/natural sciences with a strong analytical and critical mindset. If you have a solid understanding of medical concepts and the ability to keep focus on both details and the big picture, then you may be the one we are looking for. We are driven by a high level of professionalism, collaboration and an open-minded approach, where everyone contributes to an inspiring and fun working environment.

We expect that you have:

• a university degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent).
• a solid understanding of medical concepts, disease processes, scientific methodology and drug development.
• 3-5 years of experience within drug safety, pharmacovigilance or clinical development and data analysis.
• the ability to work independently in a continuous developing environment.
• a strong collaborator that are ethical, responsible, and work well under pressure when needed.
• a self-driven and strong communicator.

Become a part of ALK
In GRASP we provide an attractive working environment for individuals looking for both personal and professional development. ALK is a global pharmaceutical company in progress offering unique job opportunities.

ALK provides a uniquely dynamic and pleasant work environment, complete with inspiring and challenging assignments. You will be part of an engaged and informal team who values skill and knowledge creation, where you will be able to actively influence and challenge the status quo.

The flat structures in ALK attract independent individuals who enjoy being close to the decision-making process. We consider our pioneering spirit coupled with our trustworthiness our winning formula. Our offices in Denmark offer a green view of the DTU Science Park in Hørsholm.

Apply
Apply by attaching your CV and a short letter of motivation, no later than 6 January 2025.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We evaluate applications and call for interviews on an ongoing basis, so don't wait to apply!

If you want to know more about the position, before submitting your application, please contact Director, Alice Bjerregaard Larsen on +45 20 71 11 55.