Clinical Research Associate 2 (Biotech)

Location: Home-based in Spain; flexibility to travel is required.

Company

IQVIA Biotech supports biotech and emerging biopharma companies with clinical development services across phases and therapeutic areas.

What you will do

• Conduct site selection, initiation, monitoring, and close-out visits according to the contracted scope and applicable regulatory requirements.
• Drive and track subject recruitment plans and monitor study progress, including submissions, approvals, enrollment, CRF completion, and data query resolution.
• Provide protocol and study training to assigned sites and maintain regular communication to manage expectations and resolve issues.
• Evaluate site quality and protocol compliance, escalating issues when appropriate.
• Maintain site management documentation, visit reports, follow-up letters, TMF records, and ISF compliance.
• Collaborate with study team members and, where applicable, support site-level recruitment planning and financial management.

Requirements

• Bachelor’s degree in a scientific or healthcare discipline preferred, or an equivalent combination of education, training, and experience.
• At least 1.5 years of on-site monitoring experience.
• Knowledge of Good Clinical Practice and International Conference on Harmonization guidelines.
• Strong organizational, time management, and problem-solving skills.
• Ability to build effective working relationships with coworkers, managers, clients, and clinical trial sites.
• Must be based in Spain; flexibility to travel and a valid driver’s license are required.

Culture & Benefits

• Home-based work arrangement in Spain.
• Exposure to multiple therapeutic areas, including oncology, hematology, and cardiovascular studies.
• Work with biotech and emerging biopharma companies across clinical development phases.
• Collaborative culture supported by an agile organizational structure and therapeutic expertise.