Central Monitor in Brazil

IQVIA

São Paulo

Remote

BRL 90,000 - 130,000

Full time

2 days ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

IQVIA is seeking a Central Monitor to support remote projects across sites and teams, reviewing structured data outputs and access to medical charts to ensure data quality and patient safety.

The role requires a life sciences degree or nursing qualification, 2+ years of monitoring experience, advanced Excel, and advanced English. This is a home-based position with collaboration across Latin America and North America, and offers growth opportunities.

Qualifications

  • Bachelor's degree in life sciences or related field, or nursing qualification; or near to obtain the degree.
  • 2+ years of centralized/monitoring experience (on site or remote).
  • Advanced level of Excel and English proficiency.

Responsibilities

  • Perform centralized monitoring activities on assigned projects and evaluate data quality and study integrity.
  • Maintain internal systems and tracking tools for project-specific information.
  • Review site data, perform data trend analyses, and triage data issues with cross-functional teams.
  • Escalate quality issues to Central Monitor Lead and collaborate with sites/CRA to ensure readiness.

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.

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.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Central Monitor in Brazil
Central Monitor in Brazil

QPL IQVIA RDS Poland Sp. z o.o. • São Paulo

Remote
BRL 324,000 - 487,000
Central Monitor in Brazil
Central Monitor in Brazil

IQVIA • São Paulo

Remote
BRL 381,000 - 598,000
Sr. CRA 3, Brazil, IQVIA Biotech
Sr. CRA 3, Brazil, IQVIA Biotech

IQVIA • São Paulo

On-site
BRL 180,000 - 260,000
CRA 1
CRA 1

BZL IQVIA RDS Brasil Ltda • São Paulo

On-site
BRL 120,000 - 180,000
Sr. CRA 1, Brazil
Sr. CRA 1, Brazil

IQVIA • São Paulo

On-site
BRL 90,000 - 130,000
CRA 1
CRA 1

IQVIA • São Paulo

On-site
BRL 120,000 - 180,000
Competitive salary and benefits
CRA 2
CRA 2

IQVIA • São Paulo

On-site
BRL 120,000 - 180,000
Sr Cra 3, Brazil, Iqvia Biotech PCD
Sr Cra 3, Brazil, Iqvia Biotech PCD

IQVIA • São Paulo

On-site
BRL 150,000 - 210,000
Sr. Site Activation Specialist (North America team)
Sr. Site Activation Specialist (North America team)

IQVIA • São Paulo

On-site
BRL 120,000 - 180,000
Study Start up Specialist, IQVIA Biotech
Study Start up Specialist, IQVIA Biotech

IQVIA • São Paulo

On-site
BRL 90,000 - 140,000