Site Activation Coordinator, ComEx

IQVIA; Argentina; Presencial; ARS 54.663.000 - 81.996.000; Jornada completa

Descripción de la vacante

A global clinical research firm seeks a Site Activation Coordinator in Argentina to support site activation tasks related to import/export regulations. Responsibilities include managing site regulatory documents, ensuring compliance, and maintaining internal tracking systems. Ideal candidates should have a Bachelor’s degree in a related field, strong attention to detail, and good interpersonal skills.

Formación

• Bachelor’s degree required.
• Strong communication and organizational skills.
• Detail-oriented and able to multitask.
• General awareness of import/export processes.

Responsabilidades

• Perform site activation activities according to regulations and SOPs.
• Review documents for completeness and accuracy.
• Prepare and distribute site regulatory documents.
• Maintain project-specific information in internal systems.

Conocimientos

Interpersonal communication

Organizational skills

Attention to detail

Ability to work on multiple projects

Relationship building

Educación

Bachelor's Degree in International Commerce, Life sciences or a related field

Descripción del empleo

Job Overview

The Site Activation Coordinator will give support to Argentina in task related to import/export for site activation. Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.

Essential Functions

• Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. 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.

Qualifications

• Bachelor's Degree in International Commerce, Life sciences or a related field.
• Good interpersonal communication and organizational skills.
• Good attention to detail.
• General awareness of import/export process.
• Ability to work on multiple projects.
• Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com