Site Management Associate (Clinical Trials)

Psi CRO

Noord-Holland

Remote

EUR 32,000 - 42,000

Full time

14 days+
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Job summary

Psi CRO is seeking a clinical operations coordinator based in the Netherlands for a remote role. You will act as a primary contact for investigative sites and support day-to-day delivery of clinical studies with timely communication across international teams.

Ideal candidates have at least 6 months in clinical research, a Life Sciences degree, and fluent Dutch and English. Strong organization and MS Office skills are required to manage documentation and project training effectively.

Qualifications

  • Serve as a contact for investigative sites throughout clinical research projects.
  • Support sites in day-to-day delivery of clinical studies with timely communication.
  • Coordinate resolution of site-specific questions and collaboration between sites, project teams and stakeholders.
  • Support site teams with project training and access to study-related/vendor systems.
  • Track study and site activities and follow up on outstanding actions to keep projects on schedule.
  • Maintain accurate study information in relevant systems and up-to-date essential documentation.
  • Coordinate information and communication across internal teams and external partners.
  • Support project meetings by drafting agendas, taking minutes, and following up on actions.

Responsibilities

  • 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.

Skills

Organizational skills
Planning skills
Detail-oriented
Multitasking
Problem-solving
Teamwork
Interpersonal skills
Customer service

Education

Life Sciences degree

Tools

MS Office

Job description

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.

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 experiencewithin clinical research
  • Life Sciencesdegree
  • 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.

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