For Employers

IQVIA

FSP - Central Monitor in Mexico

Posted a day ago
2-5 years experience
Apply Now

Please mention DailyRemote when applying

?/100
Resume Match Score

Match your resume skills with our AI powered skill match!

Get professional review
AI Summary

The Central Monitor is responsible for the centralized review of study and site-level risk signals to ensure data quality and patient safety. They analyze clinical and operational data to identify trends and provide actionable recommendations to study teams and CRAs for risk mitigation.

Job Overview

IQVIA is seeking a highly analytical and detail-oriented Central Monitor to support risk-based monitoring activities across global clinical studies. This role is responsible for the centralized review of study and site-level risk signals, identifying trends, assessing potential issues, and recommending appropriate actions to ensure data quality and patient safety.

The Central Monitor operates within a centralized monitoring environment and works closely with Clinical Research Associates (CRAs), study teams, and sponsor Risk Advisors. This position does not involve direct site contact, on-site monitoring visits, data management activities, or CRA responsibilities.

Key Responsibilities

  • Perform centralized monitoring activities for assigned global clinical studies (typically 4-5 studies simultaneously).
  • Review and assess site-level and study-level risk signals generated through centralized monitoring platforms.
  • Analyze clinical and operational data to identify trends, anomalies, risks, and potential quality issues.
  • Complete signal reviews within established timelines (typically within 5 business days of signal generation).
  • Document findings, risk assessments, and recommended actions clearly and accurately.
  • Provide actionable recommendations to study teams and CRAs for risk mitigation and issue resolution.
  • Track and follow up on identified risks to ensure recommended actions have been appropriately addressed.
  • Prepare and analyze study reports, metrics, dashboards, and presentations to support risk-based monitoring activities.
  • Collaborate with sponsor-designated Risk Advisors and cross-functional study teams to evaluate risks and support study oversight.
  • Support continuous improvement initiatives related to centralized monitoring processes and risk management strategies.

Required Qualifications

  • Bachelor's degree in Life Sciences.
  • Previous experience in: Centralized Monitoring Review, Clinical Data Review, Risk-Based Monitoring (RBM), Clinical Data Analytics, Central Monitoring Findings Review
  • Strong written and verbal communication skills,. Advanced level of English is mandatory.
  • Strong presentation skills.
  • Proficiency with Microsoft Excel, reporting tools, and data visualization platforms.

Home based role.

Please, make sure to submit your CV in English. It will be assessed by a global team.

⚠️ IQVIA contacts candidates exclusively through its official recruitment channels, including corporate email addresses ending in @iqvia.com and company-authorized recruitment platforms.

If you receive a suspicious communication claiming to be from IQVIA through unofficial channels, we recommend that you do not share any personal information and contact us through our official channels for verification.

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.

Automatically Apply to the Best Remote Jobs

Stop the endless job search. Our AI finds and applies to the best jobs for you.

Try it Now
Keep looking

Similar Jobs

See all Remote Others jobs →

AI Response Evaluator

Freelance France, Japan, Mexico +3 more $10K – $20K Others

Director, Global Key Account Management

Full Time United States $165K - $180K per year Others

Director of Denials Management

Other France $80000 - $100K per year Others

Senior Field Applications Specialist (Territory: Central New York)

Full Time United States $40 - $46 per hour Others

Shared Living Provider - Norwood/Dedham/Westwood

Other United States Others

Shared Living Provider - Haverhill

Other United States Others
Apply Now

Personalize your Remote Job Search in 3 Easy Steps!

Discover remote opportunities in Others

Answer easy questions

Answer easy questions

200,000+ jobs across 15+ categories

Get your best job matches

Get your best job matches

Only hand-screened, legit jobs

Find a remote job faster

Find a remote job faster

No ads, scams, or junk

I was the first applicant for a remote marketing position that got listed on the company website the same day I applied. Had an interview within 48 hours!”

Sarah J. — Sarah J. · Marketing Manager ★★★★★ Verified