Remote Regulatory Affairs Specialist - Poland (EU-CTR)

worldwide.com; Warszawa; Remote; PLN 40,000 - 60,000; Full time

Job summary

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.

Qualifications

• 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.

Responsibilities

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

Skills

Organizational skills

Planning

Written and verbal communication

Interpersonal skills

Education

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

Tools

MS-Office applications

Job description

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.