Site Activation Specialist – Clinical Trials

IQVIA; Ciudad de México; On-site; MXN 180,000 - 300,000; Full time

Job summary

IQVIA in Mexico City is seeking a site activation professional to support regulatory activities for clinical studies. Under supervision, you will perform country-level activation tasks and help maintain study documentation in accordance with SOPs, regulations and project requirements.

Responsibilities include preparing regulatory documents, informing team of document status, distributing finalized files, and updating project systems.

Qualifications

• Bachelor's degree in life sciences or related field.
• 1 year of clinical research experience as an intern or study coordinator.
• Willingness to work in the office in Mexico City.
• Good command of English.
• Strong interpersonal and organizational skills.
• Proficiency with MS Office and word processing.
• Attention to detail and understanding of the clinical trial environment.
• Ability to manage multiple projects and maintain professional relationships.

Responsibilities

• Perform site activation activities for investigative sites in assigned studies.
• Review documents for completeness, consistency and accuracy under supervision.
• Prepare site regulatory documents and inform team of document status.
• Distribute completed documents to sites and internal team members.
• Support updating and maintenance of internal systems, databases, timelines and project plans.
• Review and track progress and approval of regulatory and ethics documents.

Skills

English proficiency

Interpersonal skills

Organizational skills

Attention to detail

Multitasking

Team collaboration

Education

Bachelor's Degree Life sciences or related field

Tools

MS Office

Job description

IQVIA in Mexico City is seeking a site activation professional to support regulatory activities for clinical studies. Under supervision, you will perform country-level activation tasks and help maintain study documentation in accordance with SOPs, regulations and project requirements.

Responsibilities include preparing regulatory documents, informing team of document status, distributing finalized files, and updating project systems.