Site Activation Specialist - Regulatory & Trials

IQVIA; Ciudad de México; On-site; MXN 320,000 - 420,000; Full time

Job summary

IQVIA in Mexico City is seeking a site activation professional to perform country-level activities in line with regulations, SOPs, and project requirements. You will review documents, prepare regulatory materials, inform teams of completion, and maintain project plans and tracking tools.

The role requires English proficiency, strong communication, and the ability to manage multiple projects in a dynamic clinical research environment.

Qualifications

• Bachelor’s degree in life sciences or related field required.
• 1 year of clinical research experience as an intern or study coordinator focusing on regulatory area preferred.
• Availability to work in the office in Mexico City.
• Good command of English.
• Strong interpersonal and organizational skills.
• Attention to detail and ability to handle multiple projects.

Responsibilities

• Perform site activation activities at country level for investigative sites.
• Prepare site regulatory documents for completeness and accuracy.
• Inform team of completion of regulatory and contractual documents for each site.
• Distribute completed documents to sites and internal teams.
• Maintain internal systems, databases, and project timelines with accurate information.
• Track and follow up on progress, approvals, and release of regulatory documents.

Education

Bachelor's Degree in Life Sciences

Tools

MS Office

Job description

IQVIA in Mexico City is seeking a site activation professional to perform country-level activities in line with regulations, SOPs, and project requirements. You will review documents, prepare regulatory materials, inform teams of completion, and maintain project plans and tracking tools.

The role requires English proficiency, strong communication, and the ability to manage multiple projects in a dynamic clinical research environment.