Remote Regulatory Affairs Specialist - Poland (EU-CTR)

worldwide.com; Warszawa; Teletrabalho; PLN 40 000 - 60 000; Tempo integral

Resumo da oferta

Worldwide Clinical Trials is hiring a Specialist in Regulatory Affairs in Warsaw, Poland. The role involves planning and submitting regulatory submissions while ensuring compliance with evolving regulations. Candidates must have a degree in a relevant science and at least three years of experience in clinical research or regulatory functions.

Strong organizational and communication skills are essential. The position is remote with opportunities for professional growth within a diverse and inclusive environment.

Qualificações

• Minimum three years of experience in clinical research or regulatory functions.
• Strong experience in the regulatory process in Poland under EU-CTR.
• Fluency in Polish is mandatory; working knowledge of English.

Responsabilidades

• Liaise with colleagues to track and submit regulatory submissions.
• Maintain country-specific drug labeling information.
• Stay informed of changing regulatory requirements.

Conhecimentos

Organizational skills

Planning

Written and verbal communication

Interpersonal skills

Formação académica

Degree in medical, biological, physical, health, pharmacy or related science

Ferramentas

MS-Office applications

Descrição da oferta de emprego

Worldwide Clinical Trials is hiring a Specialist in Regulatory Affairs in Warsaw, Poland. The role involves planning and submitting regulatory submissions while ensuring compliance with evolving regulations. Candidates must have a degree in a relevant science and at least three years of experience in clinical research or regulatory functions.

Strong organizational and communication skills are essential. The position is remote with opportunities for professional growth within a diverse and inclusive environment.