Compliance

• Process and analyze various data
• Perform administrative tasks and provide support to the firm’s internal service lines
• Prepare supporting documentation for tax returns and submissions
• Develop basic frameworks for tax calculations
• Prepare simple calculations
• Prepare tax return forms and related documents
• Maintain records of compliance work processes and files
• Prepare tax registrations and related notifications

Junior Specialist – Global Compliance and Reporting

• Build and lead team.blue’s central Compliance function within group legal
• Lead and develop Privacy Counsels, AI Counsels, and the general compliance risk-monitoring and assurance function
• Act as a first-line advisory function embedded in group legal and work alongside legal and business teams
• Drive practical implementation of regulatory requirements into business lines
• Apply a risk-based approach to prioritise compliance efforts across brands and jurisdictions
• Own the group compliance agenda for GDPR, the AI Act, the Data Act, DORA and NIS2
• Centrally coordinate the group’s Digital Services Act standard
• Set group standards, policies and playbooks and deploy them through self-serve templates and Legal Hub automation
• Anticipate incoming EU digital regulation and assess operational impact across the portfolio
• Own or coordinate sanctions, AML, conflicts of interest, third-party risk management, fraud, consumer protection and business integrity topics
• Safeguard independent judgement and provide independent oversight on escalation
• Own continuous compliance risk monitoring, assurance, regulatory watch and register-driven action
• Steer the function using KPIs such as maturity and awareness, self-serve adoption, response time and residual risk
• Partner with divisional General Counsels to embed compliance across business lines
• Foster compliance culture and enable local counsels and non-legal teams to self-serve
• Advise senior leadership and divisional GCs on compliance risk and regulatory exposure
• Work with the Sustainability Director on the digital-trust agenda and responsible-technology commitments

Head of Compliance

• Provide regulatory strategy and development guidance for clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures
• Ensure timely preparation of well-organized, quality regulatory submissions in compliance with applicable regulations
• Coordinate and prepare regulatory documents for submission to Regulatory Authorities and/or Ethics Committees
• Provide regulatory guidance throughout the clinical development life cycle
• Compile, coordinate, and review CTA/IND applications, annual reports, routine amendments, scientific advice/regulatory authority meeting materials, orphan designations, paediatric planning, and marketing applications
• Provide strategic regulatory input as required
• Develop and/or review submission documents for Regulatory Authorities and Ethics Committees
• Represent Global Regulatory Affairs at project team meetings with external and internal customers
• Work within project teams and lead regional or global projects when necessary
• Oversee and coordinate Regulatory Affairs Specialists to achieve submission targets
• Maintain project plans, project trackers, and regulatory intelligence tools; keep Regulatory Leadership updated
• Assist in developing Regulatory Affairs Specialists and other operational staff
• Provide input into regulatory strategy and timeline development for new study opportunities
• Assist in establishing company standards for high-quality submitted information
• Participate in corporate quality initiatives across Clinical Solutions business units
• Maintain and expand knowledge of laws, regulations, and guidelines governing drug development and approval
• Provide ICH GCP guidance, advice, and training to internal and external clients
• Represent Global Regulatory Affairs at business development meetings

Regulatory Manager – Senior Regulatory Manager

• Provide regulatory strategy and development guidance for clinical trials, regulatory agency meetings, orphan designations, paediatric planning, and accelerated procedures
• Coordinate and prepare regulatory documents for submission to Regulatory Authorities and/or Ethics Committees
• Provide regulatory guidance throughout the clinical development life cycle
• Compile, coordinate, and review CTA/IND applications, annual reports, routine amendments, scientific advice/regulatory authority meetings, orphan designations, paediatric planning, and marketing applications
• Develop and/or review submission documents to ensure compliance with regulatory standards
• Represent Global Regulatory Affairs at project team meetings with external and internal customers
• Work within project teams and lead regional or global projects where necessary
• Oversee and coordinate Regulatory Affairs Specialists to achieve submission targets
• Maintain project plans, project trackers, and regulatory intelligence tools; keep Regulatory Leadership updated
• Assist in developing Regulatory Affairs Specialists and other operational staff
• Contribute to regulatory strategy and timeline development for new study opportunities
• Assist in establishing company standards for high-quality submitted information
• Participate in corporate quality initiatives across Clinical Solutions business units
• Maintain and expand knowledge of drug development laws, regulations, and guidelines
• Provide ICH GCP guidance, advice, and training to internal and external clients
• Represent Global Regulatory Affairs at business development meetings

Compliance jobs in Slovakia

Junior Specialist – Global Compliance and Reporting

Head of Compliance

Regulatory Manager – Senior Regulatory Manager

Regulatory Manager / Senior Regulatory Manager