Clinical Research Associate I: Site Partnerships & Trials

Seeds Renewables; Santa Fe Capital; On-site; ARS 61,816,000 - 92,724,000; Full time

Benefits offered by this job

Health insurance

401(k) plan

Paid time off

Job summary

AbbVie seeks a clinical trial professional to advance site engagement and ensure compliant, high-quality data across trials. The role focuses on training investigators, coordinating with site staff, and supporting ongoing recruitment and study execution.

You will contribute to patient safety and regulatory compliance while collaborating across functions. Ideal candidates bring a background in health-related disciplines, 1+ year of clinical research monitoring, and strong communication skills to

Qualifications

• Bachelor's Degree in health related disciplines (Medical, Scientific, Nursing) preferred.
• Minimum of 1 year clinically related experience, including 6 months in clinical research monitoring.
• Knowledge of regulatory and ICH/GCP guidelines and applicable policies.
• Strong cross-functional collaboration skills and ability to work with diverse stakeholders.
• Ability to work in a dynamic environment with competing projects and deadlines.

Responsibilities

• Serve as primary contact for investigative sites and provide domain expertise on clinical trials.
• Align and motivate site staff and principal investigators on trial goals and patient treatment principles.
• Conduct site evaluations, training, monitoring, and closure activities per protocol and SOPs.
• Leverage CRM tools and local insights to report progress and measure engagement impact.
• Mentor and train less experienced CRAs and participate in task forces as needed.
• Monitor risk and collaborate to implement preventive and corrective actions.

Skills

Cross-functional collaboration

Planning & organization

Communication

Problem solving

Education

Bachelor's Degree in health related disciplines

Tools

CRM tool

Job description

AbbVie seeks a clinical trial professional to advance site engagement and ensure compliant, high-quality data across trials. The role focuses on training investigators, coordinating with site staff, and supporting ongoing recruitment and study execution.

You will contribute to patient safety and regulatory compliance while collaborating across functions. Ideal candidates bring a background in health-related disciplines, 1+ year of clinical research monitoring, and strong communication skills to