Global CRA: Lead International Clinical Trials

Crovelis; Madrid; Presencial; EUR 42.000 - 65.000; Jornada completa

Descripción de la vacante

CROVELIS is seeking an experienced Clinical Research Associate to join our global clinical operations team, supporting international studies with high rigor and collaboration. You will monitor sites, ensure protocol compliance, and work with investigators and staff across multiple countries.

The role demands strong GCP/ICH knowledge, independent site management, and excellent communication and organizational skills.

Formación

• Minimum 4 years of experience as a CRA in clinical trial monitoring.
• Strong experience performing Site Selection Visits (SSV) and Routine Monitoring Visits (RMV).
• Solid understanding of ICH-GCP, FDA regulations, and clinical operations processes.
• Experience managing investigative sites independently and ensuring protocol compliance.
• Ability to work in dynamic, fast-paced, international environments.
• Strong communication, organizational, and stakeholder management skills.
• Previous exposure to multicountry/global clinical trials is highly valued.

Responsabilidades

• Overseeing site performance and ensuring studies follow protocol, GCP, SOPs, and regulatory requirements.
• Conducting site qualification, initiation, routine monitoring, and close-out visits.
• Building strong relationships with investigators, coordinators, and site staff.
• Ensuring patient safety, data integrity, and overall study quality throughout the trial lifecycle.
• Reviewing source documentation, identifying protocol deviations, and supporting issue resolution.
• Collaborating closely with Clinical Trial Managers, vendors, sponsors, and cross-functional teams.
• Supporting site activation, enrollment, and retention strategies.
• Maintaining accurate and timely study documentation and monitoring reports.
• Participating in investigator meetings, trainings, and study planning activities.

Conocimientos

CRA experience 4+ years

Site Selection Visits (SSV)

Routine Monitoring Visits (RMV)

ICH-GCP & FDA knowledge

Independent site management

Communication skills

Stakeholder management

Multinational trials experience

Descripción del empleo

CROVELIS is seeking an experienced Clinical Research Associate to join our global clinical operations team, supporting international studies with high rigor and collaboration. You will monitor sites, ensure protocol compliance, and work with investigators and staff across multiple countries.

The role demands strong GCP/ICH knowledge, independent site management, and excellent communication and organizational skills.