Remote Senior Clinical Research Associate

Summary

Join our dynamic team as an experienced CRA to train and coordinate junior CRAs on site. Develop yourself as a trainer, mentor, and leader in a home-based position in Argentina.

Requirements

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Full working proficiency in Spanish and English
• Independent on-site monitoring experience in Argentina
• Experience in all types of monitoring visits in Phase II and/or III
• Availability to travel
• Experience in Oncology or Infectious Diseases is a plus
• Proficiency in MS Office applications
• Ability to plan and work in a dynamic team environment
• Communication, collaboration, and problem-solving skills

Responsibilities

• Training, mentoring and supervising study level responsibilities for Jr. CRAs
• Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits
• Delivering training of investigators, site staff and project teams
• Work with complex studies
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be involved in site identification process
• Contact for clinical investigators, vendors and support services in regard to study progress
• Participate in feasibility research
• Preparation and delivering of presentations at Investigator’s Meetings
• Preparation for and attendance at company’s audits; resolution of audit findings
• Support to Regulatory Affairs in procurement of site regulatory documents
• Maintenance of study-specific automated tracking systems