Global CTA: Regulatory Trials Technician – Barcelona

Syneos Health, Inc.; Barcelona; Presencial; EUR 34.000 - 52.000; Jornada completa

Descripción de la vacante

Syneos Health in Barcelona is seeking a Clinical Trials Technician to provide support to the Regulatory Affairs Global team. This role focuses on ensuring accuracy in data, submissions and timelines within a fast-paced environment.

You will handle pre-submission, submission and post-submission activities, update trackers, coordinate translations, verify data, and assist with archiving. Strong communication, organization and knowledge of Veeva/CTIS are essential.

Formación

• High School diploma or equivalent.
• Excellent communication skills, highly committed, detail-oriented, meticulous, and exceptionally well-organized.
• Ability to embrace new technologies.
• Experience in Veeva and CTIS.
• English very high level.
• Minimal travel up to 25% may be required.

Responsabilidades

• The CTA is a Clinical Trials Technician responsible to provide support to the Regulatory Affairs Global team.
• Main tasks: Pre-submission/submission/post-submission.
• Update Internal Timelines Tracker and notifications.
• Site Reports: Filter Excel files and verify data against official sources.
• Data Fields and Translations: Request translations for specific data fields.
• Submission Timelines Check: Verify timelines align with project requirements.
• Backlog Archiving: Address backlog related to archiving documents or data.

Conocimientos

Excellent communication skills

Detail oriented

Organized

Ability to embrace new technologies

Experience in Veeva and CTIS

English proficiency

Educación

High School diploma or equivalent

Herramientas

Veeva

CTIS

Descripción del empleo

Syneos Health in Barcelona is seeking a Clinical Trials Technician to provide support to the Regulatory Affairs Global team. This role focuses on ensuring accuracy in data, submissions and timelines within a fast-paced environment.

You will handle pre-submission, submission and post-submission activities, update trackers, coordinate translations, verify data, and assist with archiving. Strong communication, organization and knowledge of Veeva/CTIS are essential.