Central Monitor in Brazil

IQVIA; São Paulo; Remote; BRL 381,000 - 598,000; Full time

Job summary

IQVIA Inc is seeking a Central Monitor to provide remote project support across multiple studies, sites and teams, reviewing structured clinical data output with access to medical charts.

The role requires a life sciences degree, 2+ years of monitoring experience (remote or on-site), advanced Excel and strong English; this home-based position serves Latin America and North America with collaborative cross-functional interaction.

Qualifications

• Bachelor's degree in life sciences or nursing (or near completion).
• 2+ years monitoring experience (remote or on-site).
• Advanced Excel skills.
• Advanced level of English required.

Responsibilities

• Perform centralized monitoring activities on assigned projects and evaluate quality and integrity per protocol.
• Maintain internal systems, databases, and reports for project information.
• Manage triggers and prepare i-site pack for sites and countries.
• Develop basic data analytics scope and perform trend analytics where needed.
• Participate in study team meetings and coordinate with cross-functional staff.
• Escalate quality issues to Central Monitor Lead.
• Review Subject Level Data for accuracy and readiness for next review.
• Interact with sites/CRAs and follow up on milestones from start to closeout.
• Backup and perform tasks as delegated by Central Monitor Lead.

Skills

Monitoring experience

Excel

English

Education

Bachelor's degree in life sciences or nursing

Job description

São Paulo, Brazil

Mexico City, Mexico

Buenos Aires, Argentina

Bogota, Colombia

Full time

R1571881

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 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.

#LI-Remote #LI-NRJ

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.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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