Site Management Associate IFull-timeCompany DescriptionWe are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.At PSI, we believe in investing in people. Whether you're just starting your career or looking to grow within clinical research, you'll find opportunities to learn, develop and make a meaningful impact.Job DescriptionAs a Site Management Associate I (SMA I), you will play an important role in supporting the successful delivery of clinical trials. You will work closely with clinical research sites, internal project teams and international colleagues while gaining valuable exposure to the day-to-day operations of clinical studies.This position is an excellent entry point into Clinical Operations and provides a strong foundation for future career growth within clinical research.Your responsibilities will include:Maintaining clinical trial databases, tracking systems and study documentationCoordinating the collection, processing, filing and management of essential study documentsSupporting communication between investigative sites, project teams, vendors and internal departmentsServing as a primary contact for study sites regarding administrative and operational mattersCoordinating site access to study systems and supporting training activitiesAssisting with site queries and ensuring timely follow-upManaging incoming correspondence and routing information to the appropriate stakeholdersSupporting project teams with meeting preparation, agendas and meeting minutesContributing to the smooth execution of clinical research projects across different therapeutic areasQualificationsBachelor's or Master's degree in Life Sciences or a related fieldIs a recent graduate or early-career professional eager to build a career in clinical researchHas strong organizational and planning skillsIs detail-oriented and able to manage multiple priorities in a fast-paced environmentDemonstrates a proactive, solution-oriented mindsetHas strong communication and interpersonal skillsIs fluent in Dutch and English; knowledge of French is considered an assetIs comfortable working with Microsoft Office applications, including Word, Excel and PowerPointEnjoys working in a collaborative and international environmentAdditional InformationAt PSI, many professionals have started their careers in entry-level Clinical Operations roles and successfully progressed into positions such as Clinical Research Associate (CRA), Senior Clinical Research Associate and other specialized functions.We offer:Comprehensive onboarding and trainingMentorship from experienced clinical research professionalsInternational exposure and collaborationOpportunities for professional growth and developmentA supportive and people-focused cultureThe chance to contribute to studies that help improve and save patients' livesMake 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.By clicking the link above or any third-party link within this posting, you are leaving this site and going to a third-party website where the third-party website's terms and privacy policy applyI'm interestedI'm interestedPrivacy Notice
