Senior Clinical Research Associate II - Barranquilla

Syneos Health, Inc.; Colombia; On-site; COP 60,000,000 - 90,000,000; Full time

Job summary

Syneos Health, Inc. in Barranquilla, Colombia seeks a CRA II or Sr CRA for real-world late phase monitoring. The role focuses on site initiation, monitoring, data integrity and regulatory compliance, with travel up to 75%.

The candidate should have strong GCP knowledge and hands-on monitoring experience within a global CRO setting. This position emphasizes collaboration with site staff, sponsor teams and cross-functional groups to ensure audit readiness and high-quality data capture across

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
• US ONLY: Deployment to sites to gain facility access may be required

Responsibilities

• Performs site qualification, initiation, interim monitoring, site management and close-out visits, on-site or remotely, ensuring regulatory and protocol compliance
• Verifies informed consent and protects subject confidentiality and data integrity
• Reviews ISF, TMF and conducts source document review; drives query resolution and data quality
• Manages IP inventory, storage, and labeling per protocol and local regulations
• Ensures site staff training and compliance with project plans
• Documents activities via letters, logs and trip reports; supports recruitment and tracking
• Communicates project scope, budgets, and timelines; adapts to changing priorities

Skills

Site management

GCP knowledge

Communication

Travel readiness

Education

Bachelor’s degree or RN

Job description

Syneos Health, Inc. in Barranquilla, Colombia seeks a CRA II or Sr CRA for real-world late phase monitoring. The role focuses on site initiation, monitoring, data integrity and regulatory compliance, with travel up to 75%.

The candidate should have strong GCP knowledge and hands-on monitoring experience within a global CRO setting. This position emphasizes collaboration with site staff, sponsor teams and cross-functional groups to ensure audit readiness and high-quality data capture across