Clinical Research Manager
2 maanden geleden
At ICON, we are committed to advancing clinical research and providing outsourced services to pharmaceutical, biotechnology, medical device, and government organizations.
Job Summary:
We are seeking a highly skilled 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 research protocols, clinic budgets, case report forms, informed consent forms, and study volunteer information.
- Participates in the assessment, preparation, and implementation of studies for the clinic to ensure 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, and coordinates in- and outpatient visits.
- Serves as liaison between all clinic groups and 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, and communicates any changes in scope and/or cost.
- Monitors study timelines and output by clinic staff according to protocol and internal procedures.
Benefits of Working at ICON:
We offer 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.
Equal Opportunities Employer:
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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