Site Activation Specialist: Regulatory & Study Coordination

IQVIA LLC; Ciudad de México; Presencial; MXN 320.000 - 480.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Regulatory Site Activation professional in Mexico City to perform regulatory and site activation tasks within local and international guidelines. You will review documents, prepare regulatory materials, and coordinate with the Project Management team and SAM to ensure compliant site activation across studies.

The role requires office availability, strong communication, and attention to detail.

Formación

• Bachelor's Degree Life sciences or a related field.
• 1 year of clinical research experiences as an intern or study coordinator who wants to develop in the regulatory area.
• Availability to go to the office.
• Living in Mexico City.
• Good interpersonal communication and organizational skills.
• Good word processing skills and knowledge of MS Office applications.
• Good attention to detail.
• General awareness clinical trial environment and drug development process.
• Ability to work on multiple projects.Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.

Responsabilidades

• Perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions.
• Review documents for completeness, consistency and accuracy, under guidance of senior staff.
• Prepare site regulatory documents, reviewing for completeness and accuracy.
• Inform team members of completion of regulatory and contractual documents for individual sites.
• Distribute completed documents to sites and internal project team members.
• Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.
• Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.

Conocimientos

Clinical research experience

Interpersonal communication

MS Office

Attention to detail

Multi-project management

Team collaboration

Office presence

Educación

Bachelor's Degree Life sciences

Herramientas

MS Office

Descripción del empleo

IQVIA is seeking a Regulatory Site Activation professional in Mexico City to perform regulatory and site activation tasks within local and international guidelines. You will review documents, prepare regulatory materials, and coordinate with the Project Management team and SAM to ensure compliant site activation across studies.

The role requires office availability, strong communication, and attention to detail.