Eu Clinical Trial Regulatory Start-Up Specialist

Cti Clinical Trial And Consulting Services; Almada; Presencial; EUR 42 000 - 65 000; Tempo integral

Resumo da oferta

CTI Clinical Trial and Consulting Services in Portugal seeks a Regulatory Start-Up Specialist to support clinical studies from Caparica. You will review documents, ensure regulatory compliance, and interact with project teams to keep projects on track.

The ideal candidate has 3–5 years of regulatory affairs experience, a health-related degree, and strong English proficiency. This role focuses on preparing clinical trial applications and managing regulatory submissions within a dynamic CRO

Qualificações

• 3–5 years of experience in regulatory affairs.
• Fluent or proficient in English.
• Degree in a health-related field.

Responsabilidades

• Prepare clinical trial applications and submissions.
• Collaborate with project teams to ensure regulatory compliance.
• Assist in regulatory documentation and filings.

Conhecimentos

Regulatory affairs

English proficiency

Formação académica

Health-related degree

Descrição da oferta de emprego

CTI Clinical Trial and Consulting Services in Portugal is seeking a qualified professional to assist in regulatory compliance for clinical studies. The role involves reviewing documents, ensuring compliance, and interacting with project teams. The ideal candidate will have 3 to 5 years of relevant experience in regulatory affairs, proficiency in English, and a degree in a health-related field. Key responsibilities include preparing clinical trial applications and managing regulatory submissions.

Eu Clinical Trial Regulatory Start-Up Specialist Caparica, Portuguese Republic, PT