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The IRT Client Oversight Manager will oversee interactive response technology for global clinical trials, ensuring compliance with company standards. Responsibilities include maintaining project documentation, coordinating with internal and external teams, managing client relationships, and participating in bid processes and audits.

The CMC Regulatory Manager is responsible for post-approval regulatory activities related to Chemistry, Manufacturing, and Controls for biological products. Key responsibilities include preparing submission strategies, assessing change controls, ensuring compliance in study reports, and managing regulatory documentation across departments to meet quality standards.