CLINICAL TRIAL ASSOCIATE

Clinical Trial Associate – Europe – Contract We have an exciting opportunity with a European based client who’s focus on the research, development, and commercialisation of products helps patients who haven’t yet received necessary care.
You would contribute to their portfolio of life changing products as a Clinical Trial Associate in their newest facilities.
Essential Duties and Responsibilities for this role include, but are not limited to, the following.
Assist with project start-up, including development of budgets, contracts, financial disclosure statements, and grant payments.
Developing and maintaining good working relationships with Investigators and study staff.
Receive training to understand the role of a CRA to monitor sites for clinical studies.
Assist in the preparation and distribution of project status reports, newsletters, and study event memorandums.
Provide support for maintaining both electronic and paper document-tracking systems for all documents associated with the start-up and execution of clinical studies.
Desirable Experience.
Bachelor’s degree in a related discipline and related experience.
Working knowledge of ICH GCP regulations.
Experience in Pulmonary hypertension research an asset.
Experience in using basic software applications including Microsoft Office (Word - generate documents and tables, Excel - able to create and modify spreadsheets, create complex formulas, etc.) If this role is of interest to you, please apply now!     #LI-KT1