Clinical Study Manager II

4 weken geleden

Groningen, Groningen, Nederland PRA Voltijd

At ICON plc, a world-leading healthcare intelligence and clinical research organisation, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

Our mission is to accelerate the development of drugs and devices that save lives and improve quality of life. We achieve this by having a team of dedicated professionals who are passionate about their work and committed to delivering high-quality results.

The Clinical Study Manager Role:

As a Clinical Study Manager, you will be responsible for providing clinical trial management for in-house and outsourced studies. This will involve 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, coordinates 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.

Benefits of Working at ICON:

We offer a comprehensive and competitive total reward package that comprises an excellent level of base pay, a wide range of variable pay and recognition programs, best in class employee benefits, supportive policies and wellbeing initiatives. Our focus is to provide you with a workplace free of discrimination and harassment, where 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.

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