Clinical Research Associate – Remote & Travel Ready

7257 Syneos Health Argentina S.A.; Argentina; Híbrido; ARS 900.000 - 1.300.000; Jornada completa

Descripción de la vacante

Syneos Health Argentina S.A. is seeking a CRA to perform site qualification, initiation, monitoring and close-out visits, ensuring regulatory adherence and data integrity.

The role may involve on-site or remote activities with a focus on protocol compliance and patient safety. Responsibilities include overseeing informed consent, site file accuracy, and data queries, while maintaining knowledge of GCP guidelines and SOPs.

Formación

• 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.
• Excellent communication, presentation and interpersonal skills.
• Good computer skills and ability to embrace new technologies.
• Ability to manage required travel up to 75% on a regular basis.

Responsabilidades

• Performs site qualification, initiation, monitoring, management and close-out visits (on-site or remote) ensuring regulatory compliance.
• Verifies informed consent processes and protects confidentiality and data integrity.
• Reviews source documents, CRFs and data entry accuracy; guides query resolution to closure.
• Maintains knowledge of GCP/local regulations and company SOPs; supports audit readiness.
• Coordinates with project team, site staff and sponsor representatives to meet timelines.
• Assists in overseeing Investigator Meetings and site training; communicates risks and action plans.

Conocimientos

Excellent communication

Interpersonal skills

Good computer skills

Travel up to 75%

Educación

Bachelor’s degree or RN

Descripción del empleo

Syneos Health Argentina S.A. is seeking a CRA to perform site qualification, initiation, monitoring and close-out visits, ensuring regulatory adherence and data integrity.

The role may involve on-site or remote activities with a focus on protocol compliance and patient safety. Responsibilities include overseeing informed consent, site file accuracy, and data queries, while maintaining knowledge of GCP guidelines and SOPs.