Aktualne oferty pracy związane z Clinical Trial Data Reviewer - Warszawa, Mazovia - ICON
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Freelance Regional Clinical Trial Coordinator
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4 godzin temu
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5 dni temu
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Clinical Trial Finance Professional
7 dni temu
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Trial Operations Associate
3 dni temu
Warszawa, Mazovia, Polska Johnson & Johnson Pełny etatAbout the RoleWe are seeking an experienced Trial Operations Associate to join our team.In this role, you will be responsible for supporting the management of clinical trials from start-up to close-out.You will work closely with investigators, site staff, and other stakeholders to ensure that trials are managed effectively and efficiently.The ideal candidate...
Clinical Trial Data Reviewer
2 tygodni temu
Our company values diversity, inclusion & belonging. We're proud of our diverse workforce and the work we've done to become a more inclusive organisation. Our employees are at the heart of everything we do, and we're committed to providing an inclusive and accessible environment for all candidates.
We're a world-leading healthcare intelligence and clinical research organization dedicated to driving innovation and excellence. Our mission is to shape the future of clinical development. We're seeking a skilled Clinical Data Analyst to join our dynamic Medical Imaging and Cardiac Safety team.
This role is crucial in ensuring data accuracy and quality for independent read analyses, working collaboratively with Imaging Science, Project Management, and Radiology teams. You'll be instrumental in refining imaging data quality and advancing the accuracy of imaging-based data analysis.
Your key responsibilities:
- Ensuring data accuracy and quality for independent read analyses, working collaboratively with Imaging Science, Project Management, and Radiology teams.
- Refining imaging data quality and advancing the accuracy of imaging-based data analysis.
- Collaborating with Imaging Science, Project Management, and Radiology teams to ensure data accuracy and quality.
- Providing feedback on reader QC failure trends to support any necessary supplemental training.
- Performing quality checks on data exports from Independent Reads as required.
About your qualifications:
- You hold an Associate degree or bachelor's degree in Radiology and have ARRT (American Registry of Radiologic Technology) Certification.
- You have experience in imaging and a keen understanding of clinical trials and regulated environments; preferred CRO or Pharma.
- Strong organizational skills enable you to manage criteria checks, post-read QC, and documentation within defined study protocols.
- You are proficient in Microsoft tools: Excel, Word, and Outlook.