This is an excellent opportunity to build broad clinical operations experience, working directly with investigative sites and international project teams, with opportunities to develop further within clinical research.
The scope of responsibilities will include:
Serve as a key point of contact for investigative sites throughout clinical research projects.
Support sites in the effective day-to-day delivery of clinical studies, ensuring timely communication and follow-up.
Coordinate resolution of site-specific questions and facilitate collaboration between sites, project teams and other stakeholders.
Support site teams with project training and access to study-related and vendor systems.
Track study and site activities, follow up on outstanding actions and help keep projects on schedule.
Maintain accurate study information in relevant systems and ensure essential documentation is complete and up to date.
Coordinate information and communication across internal teams and external partners.
Support project meetings by drafting agendas, taking minutes, following up on agreed actions.
At least 6 months of experience within clinical research
Life Sciences 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.
We 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.
This remote position is open to candidates based anywhere in the Netherlands.
PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry, originating in Switzerland as a privately owned, full-service firm. The company supports clinical trials across multiple countries and continents, managing comprehensive trial operations including investigator site identification, patient enrollment, monitoring, data integrity, and regulatory compliance. PSI is known for being highly selective about projects and delivering high-quality, timely services across a broad spectrum of therapeutic indications. The company also develops internal IT solutions with a focus on AI initiatives to support business processes and operations.
