Primary Duties: program/project management - need to be able to multitask, organized preparing for inspections of drugs in global clinical trials managing CAPAs/audits process integration managing vendors contract to perm can be at Lexington site instead of Cambridge site experience in Track Wise a plus GCP, systems/metrics experience (not GXP - this is an R&D role) Key areas of accountability and budget responsibility, if applicable. Under the direction of the Head of Internal & Supplier Audits, this position is responsible for supporting the overall execution of the overall Internal Suppler & Audit (ISA) strategy and ensure adherence to R&D QA & Compliance (QA&C) Operational objectives.
https://www.indeed.com/job/regulatory-affairs-specialist-iii-09bfc38f993bd3f1
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