OBS! Ansökningsperioden för denna annonsen har
passerat.
Arbetsbeskrivning
<strong> The work contains/include </strong>:
• Participate in/co-ordinate the development of clinical documents such as study protocols, investigator brochures/Report of Prior Investigation and study reports
• Participate in the development of clinical documentation to support regulatory submissions and reply to questions from regulatory authorities.
• Participate in the development of risk analysis for products in development
• Manage the clinical scope of study preparation and conduct
• May serve as the primary contact with CRO and act as team leader of the study working group
• Manage clinical risk analysis for the scope of the clinical study
• Represent Clinical Development in project teams
<strong> In addition to the assignment the following tasks will or may occur: </strong>
• Participate in the development and improvement of working instructions and routines pation in the development and improvement of working instructions and routines
<strong> Education Requirements: </strong>
University degree in Biology, Chemistry, Pharmacy, or Medicine; preferably MSc or MD.
PhD is meriting.
<strong> Other Requirements </strong>
Experience in doing presentations to a scientific audience. You have experience in presenting in English as well as being fluent in English (written and oral). You should have Life Science experience and experience from all parts of the clinical trial process, from protocol development to the compilation of study reports.
You have GCP Experience and we believe you have thorough knowledge in Good Clinical Practice and clinical study execution.You have worked as a Clinical Project Manager of clinical studies in major market(s).
<strong> As a person you are: </strong>
You have courage and willingness to learn and work with new things as well as being agile/flexible to changes. You are known to adapt in a changing environment and have a strong sense of accountability.
<strong> About our client </strong>
Our client in Uppsala has a unique edge - our client works with the whole product chain from research and development to production and marketing. We are offering you the opportunity to work in an exciting, international environment where both professional and personal development is encouraged. We are based in modern offices and located in Uppsala only a 10-minute bike ride from Uppsala Central Station.
Kontaktpersoner på detta företaget
Sara Jupiter
Emma Bergman
08 555 540 09
Natalie Squalli
Margot Estlander
08-555 651 24
Margot Estlander
Karl Engström
Margot Estlander
08 555 651 24
Joacim Jonasson
08 555 651 26
May Molin
08-55565017
Joacim Jonasson
08-555 651 26