Senior Clinical Research Associate

This is a fully remote position, open to applicants in Mexico.

📋 Description

• Train and oversee junior CRAs on-site

• Prepare, execute, and report on selection, initiation, routine, and closeout monitoring visits

• Provide training to investigators, site personnel, and project teams

• Handle complex studies

• Conduct CRF review, source document verification, and resolution of queries

• Manage communication and oversight at sites

• Participate in the site identification process

• Serve as the point of contact for clinical investigators, vendors, and support services regarding study advancements

• Engage in feasibility studies

• Prepare and present at Investigator’s Meetings

• Prepare for and attend company audits; address any audit findings

• Assist Regulatory Affairs in obtaining site regulatory documents

• Maintain automated tracking systems specific to the study

⛳️ Requirements

• Degree from a college or university in Life Sciences or a related field

• Full working proficiency in both Spanish and English

• Minimum of 3 years of independent on-site monitoring experience in Mexico

• Experience with all types of monitoring visits in Phase II and/or III

• Willingness to travel

• Experience in Oncology or Infectious Diseases is an advantage

• Proficient in MS Office applications

🏝️ Benefits

• Opportunities for professional development

• Customized courses and mentoring

• Health insurance

• Paid time off