Clinical Data Manager jobs in The Netherlands
Clinical Data Manager jobs involve managing and organizing the data collected during clinical trials or research studies. These professionals ensure the accuracy, integrity, and confidentiality of clinical data and play a critical role in ensuring data quality and compliance with regulatory requirements. Clinical Data Managers work closely with cross-functional teams, including researchers, biostatisticians, and data entry personnel, to design and implement data collection systems, develop data entry guidelines and validation checks, and oversee data entry and cleaning processes. They may also develop and maintain electronic databases, design case report forms, and generate data management plans. Clinical Data Managers are responsible for data validation, resolving data discrepancies, conducting quality control checks, and ensuring that data is complete, accurate, and consistent. They may also collaborate with statistical programmers to generate analysis datasets and contribute to the preparation of study reports or publications. Clinical Data Manager jobs require a strong understanding of clinical research methodologies, data management principles, and regulatory guidelines, such as Good Clinical Practices (GCP) and Clinical Data Interchange Standards Consortium (CDISC) standards. These professionals need excellent attention to detail, organizational skills, and the ability to work with various data management software and tools. Clinical Data Managers play a crucial role in the successful execution of clinical trials and contribute to the overall integrity of clinical trial
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- Analyst II, Medical Writing, ImmunologyJohnson & Johnson - Leiden, Netherlands; Beerse, Belgium3 days old
- Manager, Site SAP Data Maintenance and System ProcessBristol Myers Squibb - Leiden, Netherlands10 days old
- Senior Specialist, QA OperationsBristol Myers Squibb - Dublin, Ireland; Utrecht, Netherlands11 days old
- Analyst II, Regulatory Medical Writing X-TAJohnson & Johnson - Leiden, Netherlands; Beerse, Belgium17 days old
- Medical Information and Adverse Event Intake Specialist with German and English languageIQVIA - Oeiras, Portugal22 days old
- Senior Manager/Associate Director, Regulatory Medical Writing X-TAJohnson & Johnson - Leiden, Netherlands; Beerse, BelgiumPosted 30+ days ago
- Director, CRO Excellence and Process Innovation LeadGenmab - Utrecht, Netherlands; Copenhagen, Denmark; Princeton, United StatesPosted 30+ days ago
- Analyst II, Medical Writing, ImmunologyJohnson & Johnson - Leiden, Netherlands; Beerse, BelgiumPosted 30+ days ago
- Associate Director, BioStatisticsGenmab - Utrecht, Netherlands; Copenhagen, DenmarkPosted 30+ days ago
- Global Feasibility Lead (Italy, UK, France, Spain, Portugal, Belgium,, Austria) - Sponsor-dedicatedSyneos - Amsterdam, NetherlandsPosted 30+ days ago
- Contract Negotiator (FSP) NetherlandsIQVIA - Amsterdam, Netherlands; Breda, NetherlandsPosted 30+ days ago
- Associate Director, BistatisticsGenmab - Utrecht, Netherlands; Copenhagen, DenmarkPosted 30+ days ago
- Manager X-TA, Regulatory Medical WritingJohnson & Johnson - Leiden, Netherlands; Beerse, BelgiumPosted 30+ days ago
- Associate Director, X-TA Regulatory Medical WritingJohnson & Johnson - 7 LocationsPosted 30+ days ago
- Associate Director, Global Trial LeadGenmab - Utrecht, Netherlands; Copenhagen, Denmark; Princeton, United StatesPosted 30+ days ago