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The Senior Director will partner with the EVP of Global Quality to develop and execute global quality and compliance strategies across clinical research services. They will lead quality transformation initiatives, oversee regulatory inspections, and manage a team of quality leads to ensure operational excellence and inspection readiness.
The Senior Director is responsible for driving business development, managing key client relationships, and overseeing strategic consulting engagements. They lead cross-functional teams to deliver expert guidance on RWE, HEOR, and market access while fostering internal innovation.
The Regulatory Submission Manager leads operational submission execution for clinical trial applications and acts as the regional regulatory representative within study teams. They are responsible for driving global submission strategies, managing documentation, and ensuring compliance with industry and agency guidelines.
Provide expert legal analysis on the EU AI Act, GDPR, and data governance to support AI model training and compliance. Identify legal inaccuracies in AI-generated responses and develop structured legal reasoning and evaluation criteria.
The Senior Compliance Specialist manages GxP regulatory authority inspections across the EMEA region, providing consultation on inspection readiness and preparation. They also support project teams in investigating non-conformances, developing CAPAs, and facilitating post-inspection follow-up activities.
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The Legal & Compliance Officer will support the Head of Legal in managing regulatory compliance, licensing obligations, and internal corporate policies. Responsibilities include conducting B2B KYC processes, monitoring responsible gambling activities, and assisting with internal and external audits.
The Compliance Officer will support legal and compliance operations, ensuring adherence to iGaming regulations, licensing requirements, and internal policies. Responsibilities include managing B2B KYC processes, drafting corporate documents, monitoring licensing obligations, and assisting with internal audits.
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 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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