Clinical Study Manager II
4 dagen geleden
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.
- Reviews and assesses research protocols, clinic budgets, case report forms, informed consent forms, and study volunteer information.
- Participates in the assessment, preparation, and implementation of studies to ensure timely and high-quality study output.
- Conducts feasibility analysis, reviews availability and workload for study volunteers, and creates risk analysis and contingency plans.
- Serves as liaison between clinic groups and management, communicating changes in scope and/or cost and escalating issues or major deviations.
- 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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