Sr. Manager, Centralized Monitoring, Risk-Based Monitoring (RBM) & Risk-Based Quality Management (RBQM)

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8 Locations
In-Office or Remote
Senior level
Biotech
The Role
Lead and oversee centralized and risk-based monitoring activities across global clinical studies. Identify risks, trends, and safety concerns, drive risk assessments, monitoring plans, analytics, dashboards, and data-driven strategies. Partner with study teams and sponsors, ensure ICH-GCP and regulatory compliance, and support continuous process improvements and sponsor-facing activities.
Summary Generated by Built In

Sr. Manager, Centralized Monitoring, Risk-Based Monitoring (RBM) & Risk-Based Quality Management (RBQM) – Latin America

At Fortrea, we are advancing clinical trials through innovative, risk-based approaches and data-driven oversight. We are looking for an experienced Sr. Manager, Centralized Monitoring, Risk-Based Monitoring (RBM) & Risk-Based Quality Management (RBQM) to be part of a high-performing team and drive centralized monitoring activities across global clinical studies.

What You'll Do
  • Oversee site-, regional-, and study-level centralized monitoring and risk-based monitoring activities.
  • Review and identify risks, trends, protocol deviations, and safety concerns, ensuring timely escalation and resolution.
  • Partner with Clinical Trial Leads, CRAs, Project Managers, and sponsors to support effective study oversight.
  • Drive study risk assessments, monitoring plans, analytics, dashboards, and data-driven monitoring strategies.
  • Serve as a key customer contact for assigned studies and contribute to proposals, bid defenses, and sponsor presentations.
  • Ensure compliance with ICH-GCP, regulatory requirements, and Fortrea SOPs while supporting continuous process improvement initiatives.
What We're Looking For
  • Degree in Life Sciences, Nursing, Medical Technology, or a related healthcare discipline.
  • Approximately 10–12 years of clinical research experience.
  • At least 2 years of experience in Risk-Based Quality Management (RBQM), Centralized Monitoring, or Risk-Based Monitoring (RBM).
  • Experience with RBQM analytical systems available in the market (e.g., Xcellerate, CluePoints, Spotfire, sponsor-specific platforms, etc.).
  • Strong knowledge of ICH-GCP and clinical trial regulations.
  • Strong analytical, problem-solving, communication, and stakeholder management skills.
  • Advanced MS Office skills.
  • Fluent English.
Why Fortrea?
  • Fully home-based role in Latin America.
  • Opportunity to lead global studies and influence centralized monitoring, risk-based monitoring, and RBQM strategies.
  • Collaborative international environment and strong career development opportunities.
  • Meaningful work that helps bring new therapies to patients worldwide.
Location Requirement

Candidates must be based in Latin America and have authorization to work in their country of residence.

Ready to Make an Impact?

Apply today and help shape the future of clinical trial monitoring at Fortrea!

Learn more about our EEO & Accommodations request here.

Skills Required

  • Degree in Life Sciences, Nursing, Medical Technology, or related healthcare discipline
  • Approximately 10-12 years of clinical research experience
  • At least 2 years experience in Risk-Based Quality Management (RBQM), Centralized Monitoring, or Risk-Based Monitoring (RBM)
  • Experience with RBQM analytical systems (e.g., Xcellerate, CluePoints, Spotfire, sponsor-specific platforms)
  • Strong knowledge of ICH-GCP and clinical trial regulations
  • Strong analytical, problem-solving, communication, and stakeholder management skills
  • Advanced MS Office skills
  • Fluent English
  • Based in Latin America and authorized to work in country of residence

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The Company
HQ: Durham, NC
10,811 Employees

What We Do

Fortrea (Nasdaq: FTRE) is a leading global provider of clinical development and patient access solutions to the life sciences industry. We partner with emerging and large biopharmaceutical, medical device and diagnostic companies to drive healthcare innovation that accelerates life changing therapies to patients in need. Fortrea provides phase I-IV clinical trial management, clinical pharmacology, differentiated technology-enabled trial solutions and post-approval services. Fortrea’s solutions leverage three decades of experience spanning more than 20 therapeutic areas, a passion for scientific rigor, exceptional insights and a strong investigator site network. Our talented and diverse team working in more than 90 countries is scaled to deliver focused and agile solutions to customers globally. Learn more about how Fortrea is becoming a transformative force from pipeline to patient at Fortrea.com.

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