Key skills
MentoringCommunication
About this role
Role Overview
- Train and coordinate junior CRAs on site
- Prepare, conduct, and report selection, initiation, routine, and closeout monitoring visits
- Deliver training to investigators, site staff, and project teams
- Work with complex studies
- Perform CRF review, source document verification, and query resolution
- Manage site communication and management
- Be involved in site identification process
- Contact for clinical investigators, vendors, and support services regarding study progress
- Participate in feasibility research
- Prepare and deliver presentations at Investigator’s Meetings
- Prepare for and attend company audits; resolve audit findings
- Support Regulatory Affairs in procuring site regulatory documents
- Maintain study-specific automated tracking systems
Requirements
- College/University degree in Life Sciences or equivalent
- Full working proficiency in Spanish and English
- At least 3 years of independent on-site monitoring experience in Mexico
- Experience in all types of monitoring visits in Phase II and/or III
- Availability to travel
- Experience in Oncology or Infectious Diseases (a plus)
- Proficiency in MS Office applications
Benefits
- Professional development
- Tailored courses and mentoring
- Health insurance (implied)
- Paid time off (implied)