Clinical Study Manager II

6 dagen geleden

Groningen, Groningen, Nederland PRA Voltijd

Clinical Study Manager II Role


At ICON plc, we are looking for a Clinical Study Manager II to join our team in Groningen, Netherlands. As a Clinical Study Manager II, you will be responsible for providing clinical trial management for in-house and outsourced studies, performing quality checks, protocol and document development, and executing study delivery plans aligned with program goals and timelines.



Key Responsibilities



  • Reviews and assesses the research protocol, clinic budget, case report forms, informed consent forms, and study volunteer information.
  • Participates in the assessment, preparation, and implementation of studies for the clinic to ensure a timely and high-quality study output.
  • Conducts feasibility analysis, reviews availability and workload for study volunteers, practicability, and required personnel, creates risk analysis, and contingency plans.
  • Coincides in- and outpatient visits, serves as liaison between all clinic groups and the applicable clinic management, communicates any changes in scope and/or cost, and escalates issues and/or major deviations.
  • Serves as clinic contact for the study sponsor, prepares and reviews clinic documents, ensures proper sampling, collection, and transmission of research data samples.
  • Monitors the study timelines and output by clinic staff according to protocol and internal procedures.


What You Will Gain



  • A unique opportunity to learn the CSM role and the context of Early Phase Clinical Research.
  • The chance to assist the CSM team with all of the above role responsibilities across a broad range of study and population types, including patient research.


Working at ICON


Our success depends on the knowledge, capabilities, and quality of our people. We are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.


At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises not only an excellent level of base pay but also a wide range of variable pay and recognition programs. In addition, our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career – both now and into the future.


ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.


If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process or in order to perform the essential functions of a position, please let us know.


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