Clinical Study Manager II

4 dagen geleden


Groningen, Groningen, Nederland Icon plc Voltijd

Clinical Study Manager II Job Summary

At ICON plc, we're proud to foster an inclusive environment driving innovation and excellence. We're seeking a Clinical Study Manager II to provide clinical trial management for in-house and outsourced studies.

  1. Reviews and assesses research protocols, clinic budgets, case report forms, informed consent forms, and study volunteer information.
  2. Participates in the assessment, preparation, and implementation of studies to ensure timely and high-quality study output.
  3. Conducts feasibility analysis, reviews availability and workload for study volunteers, and creates risk analysis and contingency plans.
  4. Serves as liaison between clinic groups and management, communicating changes in scope and/or cost and escalating issues or major deviations.
  5. Prepares and reviews clinic documents, ensures proper sampling, collection, and transmission of research data samples, and monitors study timelines and output by clinic staff.

Requirements

  • Bachelor's degree in life sciences, pharmacy, or a related field; advanced degree preferred.
  • Previous experience in clinical research, preferably within the CRO or pharmaceutical industry.
  • Understanding of clinical trial regulations, guidelines, and industry standards.
  • Strategic thinking and problem-solving abilities with a focus on driving results.
  • Excellent leadership and communication skills, with the ability to effectively manage cross-functional teams.
  • Fluent in Dutch and English.

About ICON

We offer a competitive salary, a range of additional benefits, and opportunities for career growth and development. Our benefits include various annual leave entitlements, health insurance offerings, competitive retirement planning, and a global Employee Assistance Programme. Join us in shaping the future of clinical development and fostering an inclusive environment driving innovation and excellence.


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