Clinical Research Associate II - Lisbon | Growth & Travel

Cross Border Talents; Lisboa; On-site; EUR 45,000 - 60,000; Full time

Benefits offered by this job

Company car

Mobile phone

Attractive benefits package

Job summary

IQVIA is seeking a Clinical Research Associate 2 based in Portugal. The role focuses on site visits, patient recruitment planning, and ensuring site quality according to GCP/ICH guidelines. You will track submissions, recruitment, data queries, and collaborate with study sites and client teams.

The ideal candidate holds a science/healthcare degree, has 2–4 years of on-site monitoring experience, and is fluent in Portuguese and English, with strong MS Office skills and travel flexibility.

Qualifications

• 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

Responsibilities

• 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, i.e., Good Clinical Practice and International Conference on Harmonization 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

Skills

Portuguese & English fluency

Organizational skills

Time management

Communication skills

Problem solving

Travel flexibility

Education

University degree in science/healthcare

Tools

MS Office

Job description

IQVIA is seeking a Clinical Research Associate 2 based in Portugal. The role focuses on site visits, patient recruitment planning, and ensuring site quality according to GCP/ICH guidelines. You will track submissions, recruitment, data queries, and collaborate with study sites and client teams.

The ideal candidate holds a science/healthcare degree, has 2–4 years of on-site monitoring experience, and is fluent in Portuguese and English, with strong MS Office skills and travel flexibility.