We are looking for the best and the brightest CRA's to join our Site Intelligence and Activation team. Contact us now to discuss your application further and to find out where a career at PPD can take you!
You will work on awarded projects alongside the Country Approval Specialist, and Contract Specialist within our Brussels office. The role will facilitate effective communication between investigational sites and the PPD project team. Primary responsibilities will include identifying investigators, site evaluation, producing pre study visit reports and collection of essential documents. Other responsibilities may include the support of the Site Intelligence and Activation team in activities related to the Ethics Committees submission and the preparation of Regulatory Compliance Review packages.
You will play a key part in coordinating the rapid start up phase of studies and as such will spend a significant amount of working time on site. You must possess excellent communication and interpersonal skills to enable you to develop key relations with site staff. In addition, you will need strong attention to detail with the ability to work independently. You will be authorised to perform PSVs and be able to demonstrate effective evaluation visits. QualificationsRequired Education and Experience Bachelor's or higher graduate degree in a science related field, licensed or certified health care training or equivalent experience Valid driving license English, Dutch and French language Experience as a Clinical Research Associate / monitor or in a health sciences field / clinical research setting is preferred. Desired Education and Experience Basic medical/therapeutic area knowledge and medical terminology preferred. The position will be based in our Brussels office, and can be either office based or homebased (depending on experience) *LI-LS1