Clinical Trial Coordinator – English Only

Acerca de la Empresa

IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to accelerating innovation and driving healthcare forward by leveraging data, technology, and human expertise. With a presence in over 100 countries, IQVIA helps clients develop and commercialize medical advancements that improve patient outcomes, focusing on improving patient health worldwide.

Descripción del Trabajo

As a Clinical Trial Coordinator (CTC) at IQVIA in San Sebastian, you will play a crucial role in the successful execution of clinical trials. This position requires strong organizational skills, meticulous attention to detail, and excellent communication abilities, primarily in English. You will support clinical research teams by managing study documentation, coordinating site activities, and ensuring compliance with protocols and regulatory requirements. This is an excellent opportunity for individuals passionate about contributing to medical research in a dynamic and supportive environment.

Responsabilidades Clave

• Manage and maintain essential clinical trial documentation, ensuring accuracy and compliance with regulatory guidelines (ICH-GCP).
• Assist with the preparation and submission of regulatory documents to ethics committees and competent authorities.
• Coordinate and schedule study-related meetings, monitor visits, and investigator meetings.
• Support trial sites with logistical tasks, including managing study supplies and equipment.
• Facilitate communication between study sites, sponsors, and internal clinical research associates.
• Track participant recruitment and progress, ensuring data entry is timely and accurate.
• Maintain accurate study trackers and databases.
• Assist with resolution of data queries and discrepancies.
• Ensure all study activities adhere to standard operating procedures (SOPs) and study protocols.

Habilidades Requeridas

• Proficiency in English (written and spoken) is mandatory.
• Strong organizational and time management skills.
• Excellent attention to detail and accuracy.
• Ability to work independently and as part of a team.
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook).
• Strong verbal and written communication skills.
• Problem-solving aptitude.

Cualificaciones Preferidas

• Bachelor's degree in a life science, healthcare, or related field.
• Previous administrative experience, preferably within a scientific or medical environment.
• Familiarity with medical terminology and clinical research processes.
• Knowledge of ICH-GCP guidelines and relevant regulatory requirements.

Ventajas y Beneficios

• Competitive annual salary and performance bonuses.
• Comprehensive health insurance package.
• Generous paid time off and holidays.
• Opportunities for professional development and career advancement.
• Access to cutting-edge clinical research technologies and methodologies.
• Supportive and collaborative work environment.
• Employee wellness programs.

Aplicar Ahora