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Senior Analyst, Clinical Trial Transparency Anonymization
3 tygodni temu
equire anassociated
Typical Accountabilities and required competencies
Create Anonymized Clinical Documents following best practices and established SOPs. Contribute to the Anonymization Report for the reports created. Be a system expert in the use of Technology Tool for delivery of Anonymized Clinical Documents. Perform System User Acceptance Testing (UAT) as needed to grow the key tools used to do this job. Understands the data collected and used in the Clinical Study lifecycle from site through to Clinical Document authoring. Work closely with the Biometrics Data Operations Data De-Identification Team on Risk Measurement and quantification of datasets. Accountable for good Information Practice on all assigned activities Maintain high level of understanding of regulatory policies and support protection of personal information Support development of any training materials as needed in collaboration with direct manager. Ensures adherence to all applicable AstraZeneca requirements, including but not limited to clinical operations, quality, and data privacy. Demonstrates a high focus on quality and the ability to meticulously quality check work delivered. Work with a continuous improvement mindset, looking for opportunities to improve the process and increase delivery efficiencies as this capability grows. Support the delivery of any and all Clinical Trial Transparency activities at AstraZeneca as assigned.
Essential
Desirable
Current knowledge of other technical and regulatory requirements relevant to the role. Good understanding of Global Medicines Development Knowledge of Best practices in Validated systems delivery Prior relevant knowledge of a statistical or database programming language (preferably SAS). Medical writing experience, turning Tables Figures and Listings into Clinical documents such as Clinical Study Reports (CSRs)Date Posted
14-maj-2024Closing Date
07-cze-2024-
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