This is what you will do:
The Associate Director, Clinical Trial Transparency serves as a subject matter expert and advisor on global transparency needs. This role will ensure that all clinical study registrations and information are accurately routed, tracked, and entered in appropriate databases as per regulatory requirements and in line with Alexion principles, policies, standards, and the law. This role will process clinical documents for anonymization and/or pseudo anonymization in support of Health Canada's PRCI process, EMA policy 0070, EU Clinical Trial Regulation (CTR) and other disclosures of clinical documents that must be redacted or otherwise anonymized to support results posting in public registries and/or any other specific need (eg. publications, synopsis). The role will ensure that the right tools and processes are used to ensure Alexion's assets are effectively protected including our patient confidentially. This position will support the overall Clinical Trial Transparency departmental goals and vision.
You will be responsible for:
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