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The Contract Manager is responsible for the full life cycle of sponsor contracts, including drafting budgets, scopes of work, and legal terms. They will collaborate with cross-functional departments to negotiate study budgets and finalize project timelines and costs.
The role involves managing regulatory compliance, licensing, and reporting across multiple licensed markets. It also requires advising internal teams and monitoring regulatory changes to assess business impact.
The IT Compliance Manager maintains compliance documentation and coordinates internal and external audits across various frameworks. They are responsible for managing security policies, overseeing access reviews, and handling customer security questionnaires.
The Regulatory Affairs Manager will lead the preparation of global clinical trial submissions and provide strategic regulatory guidance to internal and external clients. They are responsible for overseeing multiple projects, managing budgets, and ensuring high-quality regulatory performance across the clinical development lifecycle.
The Principal Regulatory Affairs Specialist will lead global regulatory strategies for clinical trials and act as a primary liaison with internal and external clients. They are responsible for coordinating regulatory submissions, managing project teams, and representing the department in client and regulatory agency meetings.
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