Patient Focused Drug Development Coordinator
7 days ago
Novo Nordisk A/S is a leader in the global healthcare industry with a rich history of innovation and commitment to improving patient lives. As a Clinical Outcome Assessment Specialist, you will have the opportunity to make a meaningful impact in the development of new treatments for patients living with serious chronic diseases.
This role is a one-year parental leave cover, based in Denmark, where our team is located. We are seeking an individual with expertise, passion, and experience in selecting, modifying, developing, and validating COAs to measure outcomes that matter to patients in clinical trials.
About the Role
You will be responsible for planning, overseeing, and reporting on in-trial patient interviews to develop and/or conceptualize a COA measure for regulatory use. You will also contribute to the development of COA dossiers and other regulatory briefing books when a product label claim is pursued based on a COA measure.
You will work closely with cross-functional teams, including Product Development Committee, Product Development Council, Global Project Team, Medical Science Team, advisory boards, health authorities, and investigator meetings to ensure regulatory decision-making.
Responsibilities
- Plan, oversee, and report on in-trial patient interviews to develop and/or conceptualize a COA measure for regulatory use.
- Contribute to the development of COA dossiers and other regulatory briefing books when a product label claim is pursued based on a COA measure.
- Contribute to COA aspects of the clinical development program for regulatory decision-making at internal and external meetings.
- Advise on the use of COAs in post-submission activities to allow successful life cycle management.
- Provide scientific support for congresses, symposia, and external collaborations related to COA.
Requirements
- A Master's degree in a relevant field such as health economics, pharmacy, public health, psychology, medicine, or epidemiology.
- Familiarity with collecting, analysing, and reporting qualitative and/or quantitative data.
- Experience in COA development and validation methods is preferred.
- Knowledge of clinical drug development and relevant regulatory guidelines is preferred.
- Excellent communication skills, both written and spoken, with fluency in English.
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