Remote Clinical Research Associate II (Spain)

IQVIA; Barcelona; Presencial; EUR 38.000 - 52.000; Jornada completa

Descripción de la vacante

IQVIA Biotech is seeking a Clinical Research Associate to support oncology, hematology and cardiovascular trials in Spain. The position is home-based in Spain, with required on-site monitoring experience and travel readiness.

Ideal candidates will hold a science or healthcare degree and demonstrate strong organizational and communication skills to manage sites, training and regulatory tasks within GCP/ICH guidelines.

Formación

• Bachelor's Degree in scientific discipline or health care preferred.
• Requires at least 1.5 years of on-site monitoring experience.
• Equivalent combination of education, training and experience may be accepted.
• Organizational, time management and problem-solving skills.
• Ability to travel and driver’s license required.

Responsabilidades

• Perform site monitoring visits in accordance with GCP/ICH guidelines.
• Drive and track subject recruitment plans with sites to support project needs.
• Administer protocol training to sites and maintain regular communication.
• Evaluate site practices for quality and regulatory compliance.
• Track regulatory submissions, recruitment, CRF completion and data queries; may support start-up.
• Ensure site documents are filed in the TMF and ISF maintained per regulations.
• Create documentation of site management, visit findings and action plans.

Conocimientos

Organizational skills

Time management

Problem-solving

Interpersonal skills

Educación

Bachelor's degree in science or healthcare

Descripción del empleo

IQVIA Biotech is seeking a Clinical Research Associate to support oncology, hematology and cardiovascular trials in Spain. The position is home-based in Spain, with required on-site monitoring experience and travel readiness.

Ideal candidates will hold a science or healthcare degree and demonstrate strong organizational and communication skills to manage sites, training and regulatory tasks within GCP/ICH guidelines.