Kiniksa Pharmaceuticals · Lexington, MA
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Kiniksa Pharmaceuticals seeks an experienced quality compliance leader to oversee compliance operations in Lexington, MA. This senior director role focuses on quality assurance and regulatory compliance within the pharmaceutical development and manufacturing environment. The position requires extensive expertise in quality systems and compliance frameworks.
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8 years as a Clinical Data Manager across 12 trials, leading data cleaning and query resolution.
Resume — Experience
Built and maintained 9 studies in Medidata Rave, including edit-check programming.
Resume — Skills
Mentions SDTM mapping support; ADaM experience not detailed.
Resume — Projects
Therapeutic areas listed don't clearly mention oncology. Confirm if you have oncology exposure.
Resume — Experience
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