Clinical Research Associate I — Growth & Global Impact

IQVIA; Lisboa; Presencial; EUR 32 000 - 52 000; Tempo integral

Resumo da oferta

IQVIA is seeking a Clinical Research Associate in Lisbon to perform site visits, support recruitment planning, and ensure regulatory compliance across study sites. You will monitor progress, manage data queries, and collaborate with site staff and client representatives to maintain trial integrity.

The role requires at least 1 year of on-site monitoring experience, strong MS Office skills, and fluency in Portuguese and English.

Qualificações

• University degree in a scientific discipline or health care.
• Minimum 1 year of on-site monitoring experience.
• Very good computer skills including MS Office.
• Excellent command of Portuguese and English.

Responsabilidades

• Performing site selection, initiation, monitoring and close-out visits after completing training period.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and ICH guidelines.
• Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions.
• Collaborating with experts at study sites and with client representatives.

Conhecimentos

On-site monitoring

MS Office

Portuguese & English

Formação académica

University degree in scientific discipline or health care

Descrição da oferta de emprego

IQVIA is seeking a Clinical Research Associate in Lisbon to perform site visits, support recruitment planning, and ensure regulatory compliance across study sites. You will monitor progress, manage data queries, and collaborate with site staff and client representatives to maintain trial integrity.

The role requires at least 1 year of on-site monitoring experience, strong MS Office skills, and fluency in Portuguese and English.