Clinical Pharmacology Specialist to join our Obesity area

• Clinical Development & Medical
• Søborg

Are you experienced in clinical pharmacology and drug development? We are looking for a Clinical Pharmacology Specialist to join Clinical Pharmacology Obesity. In this job you will be offered exciting opportunities to increase your experience within clinical pharmacology and to expand your competencies within the clinical trial life cycle from planning through conduct to reporting, working with one of the most exciting R&D pipelines you can find in the pharmaceutical industry.

Clinical Pharmacology Obesity is part of Global Development.

In Global Development, we are responsible for managing clinical drug development worldwide from early development phases to product introduction. We ensure medical and scientific documentation for clinical submissions and authorities while ensuring that the process lives up to uniform global standards, regulations and business ethics. We work in global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society.

About the department
Clinical Pharmacology Obesity is one of five departments in the Clinical Pharmacology and Translational Medicine area, complementing two other Classical Clinical Pharmacology departments, Quantitative Clinical Pharmacology and Translational Medicine in supporting the entire Novo Nordisk development portfolio from first in man trials to registration. We work as an integrated part of the global development project teams and we are operationally and scientifically responsible for the planning and execution of clinical pharmacology trials. We provide clinical pharmacology expertise to all clinical development phases including submission and post-submission phases.

The position
As Clinical Pharmacology Specialist, your main tasks are preparation of trial protocols and other clinical trial documentation, contact to investigator, involvement in data cleaning and reporting of trial results. You have a key role in driving and coordinating the activities in the headquarter study group, and you collaborate with our affiliates and external partners involved in the management of our clinical trials on a daily basis. You drive the progress of trial activities within given timelines and in accordance with the trial budget. You will interact with many internal and external stakeholders worldwide and have the opportunity to enhance your drug development skills.

The position is based in Søborg, Denmark, but may involve international travel.

Qualifications
You have at least six years experience of conducting human clinical studies, preferably clinical pharmacology trials, and you possess knowledge within clinical drug development. You have a relevant university degree and a PhD. You have a quality mindset, meet your deadlines and communicate effectively. You have experience in managing cross-functional global teams in a dynamic environment. You are a dedicated team player who inspires trust among colleagues and stakeholders. You are proficient in both written and spoken English.

Working at Novo Nordisk

At Novo Nordisk, you will work with specialists from around the world. Our ambitious teams work toward developing the next generation of care within the Novo Nordisk strategic focus therapy areas. As a growing organisation, we offer unique opportunities for personal and professional development, as well as a chance to work alongside the best in the field.

Contact
For further information, please contact Britta Bysted at +45 3079 7842.

Deadline

September 30, 2019.

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.