Site Management Associate

About the role

Start your career in clinical research, streamlining communication, maintaining systems and managing documents. The scope of responsibilities will include: Maintenance of databases and tracking systems Work with large amount of documents, including their compiling, procurement, processing, translation and filing Communication with company departments and external parties Communication point for investigative sites participating in the clinical research projects Coordination of site-specific query resolution, project training and access to vendor-related systems for site teams Receiving and routing all mails and incoming calls Assistance with meeting arrangements Preparation of draft agendas and minutes of project meetings At least 6 months of experience in administrative and documentation management within clinical research Life Sciences university degree Full professional working proficiency in Dutch and English Good organizational and planning skills Detail-oriented, able to multi-task and work effectively in a fast-paced environment Good problem-solving abilities, flexibility Team-oriented with excellent customer service and interpersonal skills, including a positive attitude to tasks and projects Proficiency in standard MS Office applications (Word, Excel and PowerPoint) Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success.

Your Match

How well this role fits your profile.

Company Intel

What employees say

Worked at Psicro? Share your experience