The Quintiles Study Start-Up Group ensures fast patient recruitment and start-up for both local studies and complex multi-site, multinational studies. This exciting and challenging role will give you the opportunity to broaden your skills and experience, whilst playing an integral role in the clinical trials process.You will perform activities associated with study site initiation process according to applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
You may participate in feasibility and/or site identification activities, interact with Ethics Committees or deal with investigator contracts.
The successful candidate will have an interest in specializing in Contracts, Site Identification, Ethics or Core Documents, combined with a Bachelor or Master degree, or equivalent, in a scientific or healthcare discipline. Knowledge of the current regulations and start up practices within the region will be a benefit however full training will be given. Travel within this role is limited. You have very good English, Dutch and French language skills.
Successful candidate should be able to communicate efficiently on different levels, be assertive and can work on several projects at once with high flexibility, be detail oriented and have excellent time management and organizational skills.
What we have to offer:
Quintiles offers attracting salary and benefit packages that will be discussed individually.