Junior Clinical Research Associate — Kickstart Your CRA Career

IQVIA LLC; Belgique; À distance; EUR 38 000 - 52 000; Plein temps

Avantages offerts par ce poste

Company car

Mobile phone

Benefits packaging

Résumé du poste

IQVIA Belgium is seeking a Junior Clinical Research Associate to join our sponsor-dedicated team. You will gain experience across therapeutic areas and build a strong career within IQVIA.

Your responsibilities include site visits, regulatory compliance assessments, tracking submissions and data queries, and collaborating with study sites and clients. Fluency in Dutch, English, and French is required, along with a Belgium-based location.

Qualifications

• University degree in scientific discipline or health care.
• Experience in Pharma Industry, and/or Clinical Trials environment.
• Very good computer skills including MS Office.
• Dutch, English and French language skills.
• Belgium based.
• 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.

Responsabilités

• Performing site selection, initiation, monitoring and close-out visits
• 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

Connaissances

Organizational skills

Time management

Problem-solving

Team collaboration

Formation

University degree in scientific discipline or health care

Outils

MS Office

Description du poste

IQVIA Belgium is seeking a Junior Clinical Research Associate to join our sponsor-dedicated team. You will gain experience across therapeutic areas and build a strong career within IQVIA.

Your responsibilities include site visits, regulatory compliance assessments, tracking submissions and data queries, and collaborating with study sites and clients. Fluency in Dutch, English, and French is required, along with a Belgium-based location.