Experience: 
Project management of clinical trials phase I-IV with experience from CRO and phase one research clinic within many different therapeutic areas.
Experience from work with daily contact to sponsors, investigators, Clinical project teams, sub contractors as well as CRA`s and auditors.
Experience from prepared applications to relevant authorities including Ethics Committee, Danish Medicines Agency and the Danish Data Protection Agency 
Have in depth experience in review of study protocols, patient information, lay mans resumes, creation of source documentation and creation and review of CRFs
10 years of working within the frame work of ICH- GCP and related legislation.
Competencies:
Result oriented with high analytical skills, quick to structure the essential challenges and tasks from a given project and well organized
Good to prioritize relationships and responsibilities.
Self initiates and goal ting maintain a good overview and thrives in a busy environment allowing thinking out of the box and professional development.
As a colleague, a good team player with ability to delegate appropriate tasks, high spirited and values an open minded work environment. Willing to accept certain risks, and to make a strong commitment in exchange for an interesting and varied work environment.             
Personal profile:
Positive, open minded, responsible, extrovert, like to take on challenges, structured. Seen as a good communicator across both educational as well as cultural differences