A great opportunity for an experienced Trial Coordinator who loves to share his/her experience and knowledge.
Within this project, you will support a study coordinator with the preparation and follow up of two clinical trials focussed on Multiple Sclerosis. You will help create worksheets, prepare the on-site visits of trial participants and are responsible for the data entry.
Support the local site personnel with two Multiple Sclerosis clinical trials
Data entry and data management
Contact with site personnel
Preparation of patient visits
Planning of Trial visits
Contact with the Sponsor
A degree in life sciences
1 to 5 years of experience in coordinating clinical trials
Good knowledge of ICH-GCP
Experience in Multiple Sclerosis is a plus but not a must
Affinity for electronic devices (Tablets, electronic questionnaires, smartwatches, etc.)
Very strong time management skills
Languages: French, English
Strong communication skills
Strong organizational skills
Salary based on your capabilities and experience
Freelance position for 1 day a month, for approx. 2 years
Existing right to work in Europe required ( please read job spec in full before applying ).
Vacancy number: 17623