Remote CRA II - Dermatology Monitoring

46 Premier Research Group SL; España; Hybride; EUR 55 000 - 75 000; Plein temps

Résumé du poste

Premier Research is seeking a Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team in Madrid. The role offers flexible work arrangements including remote, hybrid, or office-based work.

You will support dermatology studies across phases I–IV with a focus on data integrity, patient safety, and timely site monitoring. Ideal candidates have 2+ years in clinical trials, understanding of ICH/GCP guidelines, and a background in dermatology.

Qualifications

• Bachelor degree in clinical/health field or equivalent experience.
• At least 2+ years in clinical trials and independent monitoring.
• Experience in Dermatology therapy area preferred.

Responsabilités

• Delivers quality, timely monitoring reports for sponsor approval per the Clinical Monitoring Plan timelines.
• Maintains submission of expenses according to travel and expense requirements within company guidelines.
• Monitors (remote, onsite, or other approved mode of monitoring) with a focus on data integrity and patient safety per country regulations.
• Plans day-to-day activities for monitoring of a clinical study and sets priorities per site.
• Prepares for and conducts on-site qualification, study initiation, interim monitoring, and close-out visits at investigator sites as required by the monitoring plan.

Connaissances

Clinical Monitoring

Study Coordination

GCP/ICH knowledge

Formation

Bachelor's degree or higher in clinical/health field

Outils

eTMF systems

Description du poste

Premier Research is seeking a Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team in Madrid. The role offers flexible work arrangements including remote, hybrid, or office-based work.

You will support dermatology studies across phases I–IV with a focus on data integrity, patient safety, and timely site monitoring. Ideal candidates have 2+ years in clinical trials, understanding of ICH/GCP guidelines, and a background in dermatology.