Patient Reported Outcome Scientist to Global Clinical Development, Ball...

Application deadline:27-Feb-2023
Location:Ballerup2750,,Denmark
Contract type:Permanent
Job ID:745

Role Description

Can you take on the role as LEO's new specialist in patient reported outcomes?

If you are interested in development and qualification of PRO's, you now have the opportunity to take on the challenge and become LEO Pharma's new specialist within your field of expertise. You will join a team of experienced and highly skilled scientists committed to understand the mechanisms behind skin diseases and how our candidate drugs influence these mechanisms. Global Clinical Development plays an important role in the LEO Pharma strategy and You can look forward joining LEO in one of the most exciting times in our history.

Your role
You will join an international market leader within dermatology with focus on inflammatory skin diseases. We have a rich project portfolio that covers small molecules and biologics aiming at both topical and systemic treatment solutions. Your overall focus will be to further build and implement Patient Reported Outcomes in all of our clinical projects.

Your primary tasks will be to:

• Development, validation and implementation of PRO's in clinical development programs
• Support and develop the PRO measurement strategy
• Ensure instruments are fit-for-purpose including delivery of required documentation for authority (regulatory and health technology assessment) submissions
• Represent our discipline at authority and external KOL interactions
• Contribute and drive scientific publications

You will work closely with other stakeholders from Global Clinical Development, Health Economics, Market Access and Medical Affairs as well as external vendors.

A vital part of the job is also to keep yourself updated with new developments in the field of PRO's, including relevant regulatory legislation, guidelines and submission principles.

Your qualifications
You hold a Master's degree in outcomes research, public health, epidemiology or related discipline. You are interested in qualitative research. It is an advantage if you have worked within the area of patient reported outcomes within the pharma industry, however not required. You are able to communicate complex information to colleagues across the LEO organisation and to external stakeholders. You thrive on creating results via constructive collaboration.

Your new team
As PRO Specialist you will be organised in Preclinical Safety & Clinical Pharmacology in Global Clinical Development. You will join a well-functioning department of 19 colleagues responsible for PRO Strategy, PK, PK/PD, clinical pharmacology trials, biomarker assessment, toxicology and mode of action understanding of our drugs in all phases of clinical development.

Contact and application

If you have any questions or would like to know more please feel free to contact Lotte Seiding Larsen, Principal PRO Scientist, +45 2557 8066.

You do not need to upload a cover letter, but feel free to add a few sentences in your resumé or CV on why this position has interested you.

We look forward to receiving your application.

Let's pioneer together
At LEO Pharma, we help people with skin diseases live fulfilling lives by advancing dermatology beyond the skin. We drive dermatology with our knowledge, collaboration, and curiosity, and we are at the forefront of science in developing new medicines. For us, pioneering together is about constantly improving and extending what's possible for each other, our company, and our patients.

At LEO Pharma, we welcome and consider applications from all qualified candidates because we believe that our different perspectives, backgrounds, and attitudes are what enable us to make the best decisions for LEO Pharma and meet the needs of the wonderfully diverse marketplace we operate in.

For certain positions, LEO Pharma might complete a background check conducted by a third party.