OBS! Ansökningsperioden för denna annonsen har
passerat.
Arbetsbeskrivning
<strong>Description of assignment: </strong>
Responsible for quality control of patient-related clinical study data and follow up of CRO site activities.
<strong>The work contains/include:</strong>
• Compilation/review of clinical trial documents related to monitoring and site interactions (e.g. Clinical Trial Agreement, Clinical Study Protocol, Subject Information and Informed Consent forms, Monitoring Manual and other manuals, Newsletter, Investigator’s File)
• Review of submissions to ethics committee/health authorities
• CRF design and validation of database/e-CRF system
• Oversee study product and study material (order, label, shipping)
• Contact with CRO including training of CRO’s CRA
• Site/co-monitoring
• Study administration including archiving of study documentation
• Handling of clinical study data and participate in data / data base closure preparations
<strong>In addition to the assignment the following tasks will or may occur: </strong>
Participation in the development and improvement of working instructions and routines
<strong>Requirements: </strong>
University degree in Biology, Pharmacy, or Medicine or similar.
Work experience: 5-8 years
Fluent in English (written and oral) and experience from presenting in English. You have Life Science experience and experience from all parts of the clinical trial process, from planning to completion. You have worked with GCP and you have thorough knowledge in Good Clinical Practice.
<strong> Wishful mindset: </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