Senior Clinical Research Associate, Portugal (CRA 2)

Quadrante; Lisboa; Presencial; EUR 45.000 - 65.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Company car

Mobile phone

Attractive benefits package

Descripción de la vacante

IQVIA is hiring a Clinical Research Associate 2 based in Lisbon, Portugal. You will perform site selection, initiation, monitoring and close-out visits, and support subject recruitment planning, ensuring alignment with ICH-GCP standards.

You will monitor site practices for quality and integrity, track regulatory submissions, recruitment, CRF completion and data queries, and collaborate with site experts and client representatives in an international environment.

Formación

• University degree in scientific discipline or health care.
• 2-4 years of independent on-site monitoring experience.
• Very good computer skills including MS Office.
• Excellent command of Portuguese and English language.
• Organizational, time management and problem-solving skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Flexibility to travel.
• Driver's license class B.

Responsabilidades

• Performing site selection, initiation, monitoring and close-out visits.
• Supporting the development of a subject recruitment plan.
• Evaluating the quality and integrity of site practices in accordance with regulatory requirements (GCP/ICH).
• Managing progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolutions.
• Collaborating with experts at study sites and with client representatives.

Conocimientos

MS Office

Portuguese

English

Organizational skills

Time management

Problem solving

Driver's license

Educación

University degree in scientific discipline or health care

Descripción del empleo

IQVIA is hiring a Clinical Research Associate 2 based in Lisbon, Portugal. You will perform site selection, initiation, monitoring and close-out visits, and support subject recruitment planning, ensuring alignment with ICH-GCP standards.

You will monitor site practices for quality and integrity, track regulatory submissions, recruitment, CRF completion and data queries, and collaborate with site experts and client representatives in an international environment.