Regulatory Submissions & Documentation Specialist

ICON; Lisboa; Presencial; EUR 28 000 - 42 000; Tempo integral

Vantagens oferecidas por esta oferta de emprego

Various annual leave entitlements

Health insurance offerings for you and

Retirement planning offerings

Global Employee Assistance Programme (

Life assurance

Country-specific flexible benefits

Resumo da oferta

ICON plc is a leading healthcare intelligence and clinical research organization seeking a Regulatory Technician in Lisbon. You will provide operational support by preparing, organizing, and maintaining documentation required for global regulatory submissions.

Responsibilities include formatting documents, maintaining trackers, coordinating submission information, and ensuring compliance with standards. A life sciences degree and regulatory exposure are preferred.

Qualificações

• Bachelor's degree or equivalent in life sciences, pharmacy, or related field.
• Experience in regulatory affairs or document-focused roles is preferred.
• Strong attention to detail with ability to manage multiple documents and timelines.

Responsabilidades

• Prepare and format regulatory documents and submission components.
• Maintain regulatory trackers, databases and filing systems.
• Coordinate information from cross-functional teams for submissions.
• Perform quality checks for completeness and formatting.
• Assist with correspondence and documentation for health authority interactions.
• Contribute to improving regulatory processes and templates.

Conhecimentos

Regulatory affairs

Attention to detail

Documentation management

Communication

Formação académica

Bachelor's degree in life sciences or related field

Ferramentas

Document management systems

Trackers

Office software

Descrição da oferta de emprego

ICON plc is a leading healthcare intelligence and clinical research organization seeking a Regulatory Technician in Lisbon. You will provide operational support by preparing, organizing, and maintaining documentation required for global regulatory submissions.

Responsibilities include formatting documents, maintaining trackers, coordinating submission information, and ensuring compliance with standards. A life sciences degree and regulatory exposure are preferred.