EMEA On-site Clinical Monitor - German

Syneos Health, Inc.; Lembang; Presencial; IDR 1.106.417.000 - 1.508.751.000; Jornada completa

Descripción de la vacante

Syneos Health, Inc. is seeking an on-site monitor fluent in German to support global studies across diverse EMEA countries. The role involves site management, regulatory compliance, and collaboration with sponsor teams to drive study delivery.

The candidate should have at least 1 year of onsite monitoring experience, a science/healthcare degree, and strong skills in CTMS/EDC, MS Office, and communication. Travel up to 60% is expected.

Formación

• Required - German language (written and spoken).
• Minimum 1 year of onsite monitoring experience.
• BA/BS in science/health care field or nursing degree or equivalent.
• Proficient in Microsoft Office Suite (Word, Excel, PowerPoint), email/voicemail, and CTMS/EDC systems.
• Previous site management experience (in-house/on-site/Study Coordinator).
• Excellent communication, time management, organizational, documentation and customer service skills.
• Knowledge of Real World Late Phase study designs and regulations including GPP.

Responsabilidades

• Perform site management activities in compliance with SOPs and WIs.
• Ensure compliance with local regulations and ICH-GCP guidance.
• Conduct site management per SoW and SMP; identify sites and qualification.
• Manage site start-up, regulatory tasks and remote/on-site monitoring.
• Review ISF for accuracy; reconcile with TMF and archiving requirements.
• Maintain communication with site staff and project team; escalate issues as needed.
• Support audit readiness and participate in Investigator Meetings.

Conocimientos

German language

Communication skills

Time management

Organizational skills

Teamwork

Travel flexibility

Educación

BA/BS in science/healthcare or nursing

Herramientas

Microsoft Office

CTMS/EDC systems

Descripción del empleo

Syneos Health, Inc. is seeking an on-site monitor fluent in German to support global studies across diverse EMEA countries. The role involves site management, regulatory compliance, and collaboration with sponsor teams to drive study delivery.

The candidate should have at least 1 year of onsite monitoring experience, a science/healthcare degree, and strong skills in CTMS/EDC, MS Office, and communication. Travel up to 60% is expected.