Remote Clinical Research Associate – Austria

Syneos Health, Inc.; Österreich; Remote; EUR 55.000 - 75.000; Vollzeit

Zusammenfassung

Syneos Health in Austria is seeking an experienced Clinical Research Associate (CRA) for a single sponsor partnership. The role covers site qualification, initiation, monitoring and close-out visits, performed on-site or remotely, with emphasis on regulatory and GCP compliance and timely issue resolution.

Responsibilities include informed consent validation, ISF/TMF integrity, data query resolution, IP inventory where required, and collaboration with site staff.

Qualifikationen

• 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 regulatory requirements.
• Previous monitoring experience in Austria.
• Fluency in German and English.
• Excellent communication, presentation and interpersonal skills.
• Ability to travel for monitoring visits in Austria.

Aufgaben

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (on-site or remote) ensuring regulatory, ICH-GCP and/or GPP and protocol compliance.
• Verifies informed consent and protects subject confidentiality; assesses safety and data integrity at investigator sites.
• Reviews ISF for accuracy, reconciles with TMF, and ensures archiving per local guidelines.
• Documents activities and supports recruitment and data tracking; enters data into tracking systems.
• Manages project scope, budgets, timelines and site-level communications to meet objectives; travels as required.
• May liaise with study site personnel and attend Investigator Meetings and sponsor meetings.

Kenntnisse

German language

English language

GCP knowledge

Ausbildung

Bachelor’s degree or RN

Jobbeschreibung

Syneos Health in Austria is seeking an experienced Clinical Research Associate (CRA) for a single sponsor partnership. The role covers site qualification, initiation, monitoring and close-out visits, performed on-site or remotely, with emphasis on regulatory and GCP compliance and timely issue resolution.

Responsibilities include informed consent validation, ISF/TMF integrity, data query resolution, IP inventory where required, and collaboration with site staff.