Central Monitor in Brazil

IQVIA; Bogotá; Remote; COP 30,000,000 - 54,000,000; Full time

Benefits offered by this job

Home-based

Job summary

IQVIA is seeking a Central Monitor for its remote Central Monitoring Department. You will support multiple projects/sites, review structured data with access to medical charts, and ensure data quality per protocol.

The role requires a Bachelor’s in life sciences or nursing (or near completion), advanced Excel, and fluent English. This home-based position supports Latin America or North America regions.

Qualifications

• Bachelor's degree in life sciences or nursing qualification, or near to obtain.
• Advanced Excel skills required.
• Very good command of English - mandatory.

Responsibilities

• Perform centralized monitoring activities on assigned projects and evaluate quality/integrity per protocol and SOPs.
• Maintain and update internal systems, databases, and tracking tools for project information.
• Manage triggers and prepare i-site packs for sites and countries.
• Contribute to data analytics scope and trend analyses as needed.
• Interact with study teams and sites to verify information and triage data issues.
• Escalate quality issues to Central Monitor Lead/Sr. Central Monitor.

Job description

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.

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 guideline.
• Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project specific information.
• Perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned study(ies).
• May assist in developing required basic data analytics scope and performing the trend analytics for their respective study(ies).
• Participate on study team meetings and interact with cross functional staff to verify information and/or triage new data issues or prior identified action items.
• Escalate quality issues pertaining to site to respective Centralized Monitoring Lead/ Sr. Central Monitor.
• May perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy (inclusion & exclusion criteria/ IP/AE/ Labs/EOT/EOS/ End points/SAEs etc.) Review any other information as necessary to determine overall readiness of the patient information for next level review.
• Interaction with sites/CRA and follow-up on study required milestones from the project start until close out.
• May act as backup/ perform the activities as per the task list delegated by Central Monitor Expert/Centralized Monitoring Lead.

Qualifications

• Bachelor's degree in life sciences or related field, or nursing qualification; or be near to obtain the degree - Mandatory.
• +2 years of monitoring experience (on site or remote) - Mandatory.
• Advanced level of Excel.
• We are looking for someone with advanced level of English - Mandatory. You could support sites either in Latin America or North America.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.