Clinical Study Manager II

4 weken geleden

Groningen, Groningen, Nederland PRA Voltijd

At ICON, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government organizations. Our mission is to accelerate the development of drugs and devices that save lives and improve quality of life.

The Clinical Study Manager II will provide clinical trial management for in-house and outsourced studies, perform quality checks, protocol and document development, and execute study delivery plans aligned with program goals and timelines.

Responsibilities:

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.
  • Prepares and reviews clinic documents, ensures proper sampling, collection, and transmission of research data samples.

Benefits of 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, 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 an excellent level of base pay, variable pay, and recognition programs, as well as best-in-class employee benefits, supportive policies, and wellbeing initiatives tailored to support you and your family at all stages of your career.

ICON is an equal opportunity and inclusive employer, 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.

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