Lead Safety Surveillance Advisor

Do you want to play a key role in the safety surveillance activities working with clinical and post-marketing activities? Would you like to join a dedicated and empowered team of 10 safety surveillance advisors in a growing company? Apply today!

The position
Safety Surveillance is a department within Global Safety & Pharmacovigilance, 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 evaluating the product safety profile.

Your tasks include:

• lead safety surveillance deliverable for assigned products and projects
• performing signal detection and analyse large datasets  
• write or review aggregated safety reports
• perform scientific review of individual case reports
• contribute to development of clinical study protocols
• drive and participate in cross-functional groups
• communicate benefit-risk assessments to external parties
• mentoring junior colleagues by sharing expertise and knowledge.

You will work 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 and empowerment, 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 strong understanding of medical concepts, 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. 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 2 March 2025. 

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. Hence, we prefer that you do not add images in your application documents. We evaluate applications and call for interviews on an ongoing basis, so don't wait to apply! We reserve the right to take down the advert when we have found the right candidate.

Do you want to learn more about our company, we encourage you to visit us at www.alk.net. For further information regarding the position please contact Director, Alice Bjerregaard Larsen on telephone +45 20 71 11 55.

We are looking forward to hearing from you!