Clinical Research Project Coordinator — Drive Trial Timelines

Medpace; Ciudad de México; On-site; MXN 300,000 - 420,000; Full time

Job summary

Medpace in Mexico City is seeking a full-time, office-based Clinical Research Project Coordinator to join our Clinical Trial Management team. The role supports day-to-day clinical trial management and coordinates with CTM for timely, accurate task delivery.

Responsibilities include creating project timelines, compiling status reports, and coordinating meetings with sponsors and sites. Fluency in English and strong computer and communication skills are required.

Qualifications

• Bachelor's degree in a health sciences field.
• Experience as a Study Coordinator or in pharma industry preferred.
• Excellent computer (word-processing, databases, Excel, Windows), organizational, and communication skills.
• Fluency in English.

Responsibilities

• Engage in clinical trial management on a day to day level.
• Work closely with the project CTM for timely delivery of recurrent tasks consistently with a high degree of accuracy.
• Compile and maintain project-specific status reports.
• Interact with the Sponsor, study sites, and internal associates.
• Create and maintain project timelines; and
• Coordinate project meetings and produce quality minutes.

Skills

English fluency

Communication skills

Organizational skills

Computer skills

Education

Bachelor's degree in health sciences

Job description

Medpace in Mexico City is seeking a full-time, office-based Clinical Research Project Coordinator to join our Clinical Trial Management team. The role supports day-to-day clinical trial management and coordinates with CTM for timely, accurate task delivery.

Responsibilities include creating project timelines, compiling status reports, and coordinating meetings with sponsors and sites. Fluency in English and strong computer and communication skills are required.