Remote Clinical Research Associate (Austria)

Syneos Health; Lembang; On-site; IDR 1,220,256,000 - 1,830,384,000; Full time

Job summary

Syneos Health in Austria is seeking a Clinical Research Associate to support a single sponsor's trial programs. The role focuses on monitoring site performance and regulatory compliance to ensure data integrity across study activities.

You will perform site qualification, initiation, interim monitoring, close-out visits (on-site or remote), manage study documentation, and collaborate with site staff to drive timely resolution of queries while upholding ICH-GCP standards.

Qualifications

• Bachelor’s degree or RN in a related field or equivalent combination of education, training and experience.
• Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements.
• Previous monitoring experience in Austria.
• Fluency in German and English.
• Excellent communication, presentation and interpersonal skills.

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (on-site or remotely) ensuring regulatory, ICH-GCP and/or GPP and protocol compliance.
• Verifies informed consent processes and protects subject confidentiality while ensuring data integrity.
• Reviews ISF and TMF, coordinates source data verification, and supports query resolution to timelines.
• Maintains knowledge of ICH/GCP guidelines and local regulations; supports audit readiness and training as required.

Skills

German fluency

English fluency

GCP/ICH knowledge

Site monitoring experience

Communication skills

Education

Bachelor’s degree or RN in related field

Job description

Syneos Health in Austria is seeking a Clinical Research Associate to support a single sponsor's trial programs. The role focuses on monitoring site performance and regulatory compliance to ensure data integrity across study activities.

You will perform site qualification, initiation, interim monitoring, close-out visits (on-site or remote), manage study documentation, and collaborate with site staff to drive timely resolution of queries while upholding ICH-GCP standards.