Expert in Clinical Pharmacology to manage clinical drug development

• Clinical Development and Medical
• Søborg

Are you experienced in clinical pharmacology and drug development? We are looking for a Clinical Pharmacology Specialist to join Clinical Pharmacology. 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 finalisation.

About the department
Clinical Pharmacology plays a key role in the development of new drugs at Novo Nordisk. 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.

Clinical Pharmacology 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.

The position
Your title will be Clinical Pharmacology Specialist, and you play the key role in driving and managing activities in our clinical trial teams. Furthermore, a big part of the role will be collaborating with other scientific experts including your colleagues in HQ and our affiliates as well as external partners involved in the management of our clinical trials. Some of the main tasks are preparation of trial protocols and other clinical trial documentation, contact to investigators, involvement in data cleaning and reporting of trial results. You will be scientifically and operationally responsible and drive the progress of trial activities within given timelines using your scientific expertise. 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.

Qualifications
You are experienced in conducting human clinical studies, preferably clinical pharmacology trials and you possess knowledge within clinical drug development. You have a relevant university degree, complemented by a PhD degree and preferably 5+ years of relevant pharma experience. You have a quality mindset, meet your deadlines and communicate effectively. You have experience in managing cross-functional global projects 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, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact
For further information, please contact Charlotte Keller Steensberg at +45 30791641.

Deadline

11 March 2020

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.