Senior Clinical Research Associate: Monitoring & Trials

1001 Syneos Health, LLC; Argentina; Hybrid; ARS 1,200,000 - 2,000,000; Full time

Job summary

Syneos Health is seeking a Clinical Research Associate II to conduct on-site and remote monitoring of clinical studies, ensuring adherence to GCP and regulatory standards. You will develop monitoring tools, SOPs, and training materials while coordinating site visits and documentation.

You will collaborate with investigators, site staff, and cross-functional teams to ensure study success, manage multiple priorities, and maintain high-quality trial conduct across projects.

Qualifications

• Bachelor's degree in a related field or equivalent experience.
• Minimum of 2-4 years of experience in clinical research monitoring.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and regulatory requirements.
• Excellent communication and interpersonal skills.
• Ability to work independently and manage multiple priorities.
• Proficiency in using clinical trial management systems and other relevant software.

Responsibilities

• Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices, including reviewing study protocols, informed consent forms, and case report forms
• Develop and implement tools, procedures, and processes to ensure quality monitoring, such as creating monitoring plans, checklists, and templates
• Contribute to the design, implementation, and delivery of processes, programs, and policies, including participating in the development of standard operating procedures (SOPs) and training materials
• Manage defined components of projects or processes within the area of responsibility, such as coordinating site visits, tracking study progress, and resolving issues
• Ensure accurate and timely documentation of monitoring activities and findings, including writing monitoring reports, follow-up letters, and action plans
• Collaborate with cross-functional teams to support clinical trial operations, including working with investigators, site staff, and other stakeholders to ensure smooth study conduct

Skills

GCP knowledge

Attention to detail

Communication skills

Independent worker

MS Office

Education

Bachelor's degree

Tools

CTMS

Data entry tools

Job description

Syneos Health is seeking a Clinical Research Associate II to conduct on-site and remote monitoring of clinical studies, ensuring adherence to GCP and regulatory standards. You will develop monitoring tools, SOPs, and training materials while coordinating site visits and documentation.

You will collaborate with investigators, site staff, and cross-functional teams to ensure study success, manage multiple priorities, and maintain high-quality trial conduct across projects.