Clinical Pharmacology Scientific Director - Obesity & Liver Diseases
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Søborg
Are you passionate about clinical pharmacology and drug development? Are you ready to lead clinical pharmacology programmes towards regulatory submissions and support our business development activities? Would you relish the chance to support our Obesity & Liver Diseases Portfolio with your scientific insights, patient-centric approach, and strategic mindset? Then, this is your moment as we are looking for a Clinical Pharmacology Scientific Director for Clinical Pharmacology, Obesity & Liver Diseases. Apply now. Together we can create life-changing innovations for patients. The position You will be responsible for leading clinical pharmacology programmes and providing the clinical pharmacology strategy for early and late-stage development projects within Obesity & Liver Diseases. Furthermore, your key responsibilities will be to: Provide clinical pharmacology expertise to our business development project teams. Design clinical pharmacology trials as well as interpret and communicate trial results. Drive and coordinate activities in the headquarter study groups and collaborate with our affiliates and external partners involved across the value chain. Scientific communication and interactions with many internal and external global stakeholders and key opinion leaders. Clinical pharmacology summaries of submission dossiers and interactions with Health Authorities to provide clinical pharmacology input to secure approvals of new drugs. Represent Clinical Pharmacology in global project teams. Support the development of Clinical Pharmacology competences by mentoring and sharing knowledge. Qualifications To thrive and succeed, we expect you to have: Master’s degree in Life Sciences, complemented by a Ph.D. Strong knowledge within Clinical Pharmacology in pharma or biotech industry with a solid business and value chain understanding. Scientific and strategic mindset with a good understanding of clinical dosing aspects including first human dose setting and pharmacokinetic/pharmacodynamic relationships. Experience with health authority interactions. Proven track record in planning and conducting clinical trials and working in cross-functional teams in a global and dynamic environment. Proficiency in both written and spoken English. On a personal level, you are a dedicated team player who inspires trust among colleagues and stakeholders. You have a quality mindset, meet your deadlines, and communicate effectively. Independence, initiative, and innovation should always be demonstrated when prioritising, planning for and performing tasks. You have a patient-centric approach and strategic mindset. Furthermore, you thrive in a fast-paced environment with high performing colleagues. About the department The Clinical Pharmacology department is responsible for development projects within Obesity & Liver Diseases. We are a department of dedicated and highly engaged colleagues working in a flexible, collaborative, and cross-functional setting. We focus on new innovative technologies such as RNA interference as well as monoclonal antibodies, proteins, and peptides and oral administration of peptides. Clinical Pharmacology plays a key role in the development of new drugs at Novo Nordisk. We work as an integrated part of development and research project teams, being responsible for the clinical pharmacology strategy and the scientific input to clinical pharmacology trials. We provide clinical pharmacology expertise to all clinical development phases, Health Authority interactions and regulatory submissions worldwide. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Vibeke Hatorp at +45 3075 5697. Deadline 6 August 2023. We will review the applications on an ongoing basis, so we encourage you to apply as soon as possible as the advert may close before indicated deadline. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 28.6.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Forretningsudvikler
- Søborg
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