Senior Clinical Monitoring Associate I (Remote)

7257 Syneos Health Argentina S.A.; Argentina; Remote; ARS 90,873,000 - 136,310,000; Full time

Job summary

Syneos Health is seeking a Senior CRA I to perform site qualification, initiation, monitoring, and close-out visits, ensuring regulatory compliance and data integrity. The role may involve on-site or remote activities with up to 75% travel.

You will support source data verification, IP handling, and coordination with site staff. Knowledge of ICH/GCP guidelines and strong communication skills are essential to drive study success.

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.
• Must demonstrate good computer skills and be able to embrace new technologies.
• Excellent communication, presentation and interpersonal skills.
• Ability to manage required travel of up to 75% on a regular basis.

Responsibilities

• Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.
• Verifies source documents, CRF data accuracy, and conducts query resolution remotely and on site.
• Ensures IP handling, labeling, storage, and reconciliation per protocol and GMP requirements.
• Maintains ISF accuracy and archiving per TMF requirements; reports to project team on issues and action plans.
• Supports site recruitment, retention, and data tracking; communicates scope and timelines with focused site-level coordination.

Education

Bachelor’s degree or RN

Job description

Syneos Health is seeking a Senior CRA I to perform site qualification, initiation, monitoring, and close-out visits, ensuring regulatory compliance and data integrity. The role may involve on-site or remote activities with up to 75% travel.

You will support source data verification, IP handling, and coordination with site staff. Knowledge of ICH/GCP guidelines and strong communication skills are essential to drive study success.