Central Monitor in LATAM

IQVIA; Estado de México; Presencial; MXN 1,116,000 - 1,490,000; Jornada completa

Descripción de la vacante

An innovative healthcare and life sciences company is seeking a Central Monitor for a home-based position in LATAM. This role involves performing centralized monitoring activities, ensuring the quality and integrity of studies, and managing project-specific information. The ideal candidate holds a degree in life sciences or nursing and has over two years of relevant monitoring experience, alongside advanced Excel skills and proficiency in English. This is a full-time role aimed at improving patient outcomes through quality clinical research.

Formación

• Bachelor's degree in life sciences or related field, or nursing qualification; nearing degree completion.
• +2 years of relevant monitoring experience (on-site or remote).
• Advanced Excel skills.

Responsabilidades

• Perform centralized monitoring activities on assigned projects.
• Manage triggers and prepare i-site packs for studies.
• Interact with sites/CRAs and follow up on study milestones.

Conocimientos

Advanced Excel skills

Proficiency in English

Educación

Bachelor's degree in life sciences or related field

Nursing qualification or nearing degree completion

Descripción del empleo

Join to apply for the Central Monitor in LATAM role at IQVIA.

Get AI-powered advice on this job and more exclusive features.

Job Overview

A Central Monitor is a key skilled and clinically experienced team member of IQVIA Central Monitoring Department. Provides remote project support and assistance across multiple projects, sites, and teams, and reviews the structured clinical data output with access to medical charts.

Essential Functions:

• Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs, respective regulations, and guidelines.
• Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project-specific information.
• Manage triggers and prepare i-site packs for respective sites and countries for assigned studies.
• Assist in developing basic data analytics scope and perform trend analytics for their respective studies.
• Participate in study team meetings and interact with cross-functional staff to verify information and triage new data issues or prior action items.
• Escalate quality issues pertaining to sites to the respective Centralized Monitoring Lead/Sr. Central Monitor.
• Perform Subject Level Data Review requiring further investigation with the clinical site to determine overall accuracy (including inclusion & exclusion criteria, IP, AE, Labs, EOT, EOS, Endpoints, SAEs, etc.).
• Interact with sites/CRAs and follow-up on study milestones from start to close-out.
• Act as backup or perform activities delegated by the Central Monitor Expert/Centralized Monitoring Lead.

Qualifications:

• Bachelor's degree in life sciences or related field, or nursing qualification; or nearing degree completion.
• +2 years of relevant monitoring experience (on-site or remote).
• Advanced Excel skills.
• Proficiency in English at an advanced level.

This is a home-based position.

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

Seniority level

• Not Applicable

Employment type

• Full-time

Job function

• Other

Industries

• Pharmaceutical Manufacturing