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Design, execute and report scientific experiments in biopharmaceutics, manage lab activities and lead a team in pharmaceutical therapies development.

The role involves defining platform strategy, overseeing Power Platform projects, providing technical guidance, optimizing performance, and ensuring compliance with standards. Requires extensive IT experience, particularly in Microsoft Power Platform and GenAI.

The Pharmacovigilance QA Manager ensures compliance and quality oversight for PV and DV activities, supports regulatory inspections, and drives quality improvement initiatives.

Manage projects for clinical trial drug releases, write protocols and reports, approve GMP documents, and troubleshoot methods in a lab environment.

The Web Project Manager will oversee web projects in various CMS platforms, coordinating with teams, managing content, and ensuring alignment with business needs.

The Senior Analyst will execute Incentive Compensation operations, perform analytics, ensure quality assurance, manage projects, and provide insights while adhering to IC guidelines.

The Regulatory and Development Policy Manager monitors regulatory information, communicates it to teams, and develops policy strategies for the pharmaceutical industry.

Manage supplier quality and compliance activities, including onboarding, monitoring, and exit processes, with responsibilities in documentation, audits, and risk assessments.

The Therapeutic Data Strategy Director leads the creation and execution of an operational data strategy, ensuring compliance and quality in clinical data for drug development. They oversee E2E data strategy, collaborate with stakeholders, and implement standards for data management and reporting.

The Associate Director will lead GenAI solutions using the Microsoft Power Platform, overseeing delivery, defining strategies, ensuring compliance, and optimizing performance.