Risk and Monitoring Manager - Argentina​/Mexico - Remote

Who we are

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Join us!

This role coordinates cross-functional risk management and central monitoring activities for assigned clinical trials in accordance with International Council for Harmonisation Good Clinical Practice (ICH GCP) guidelines. The role supports study teams by prioritizing quality across the study and ensuring consistency within programs, therapeutic areas, and/or sponsors.

• Supports Risk-Based Quality Management (RBQM) activities within the assigned project team

• Understands the study budget and protocol content for assigned trials

• Oversees all Risk-Based Quality Management activities on assigned studies

• Supports the development of the Project Management Plan for the assigned program or study and may provide advice on the development of other functional plans

• Develops the Central Monitoring Plan for the assigned study and gains Global Project Lead (GPL) and sponsor approval

• Delivers training to study teams regarding the RBQM strategy, including study risk assessment, centralized monitoring, Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), and the overarching monitoring strategy

• Independently provides subject matter expertise for the development and maintenance of the study-level monitoring strategy required for the program or trial

• Drafts and finalizes the initial risk assessment, ensuring cross-functional involvement

• Facilitates the identification of KRIs and/or QTLs as part of the study monitoring strategy, when applicable

• Oversees the setup of the central monitoring dashboard and central monitoring reviews performed throughout the study, when applicable

• Supports the GPL in ensuring compliance with cross-functional review of risks throughout the trial

• Performs central monitoring activities, when applicable, including review of study- and site-level KRIs and study-level QTLs, review of system outputs, identification of outliers, trends, or signals, and proposal of actions for assessment by the study team

• Follows up with study teams as appropriate for action or issue resolution

• Completes User Acceptance Testing (UAT) of RBQM technology, when applicable

• Maintains the Risk Library

• Ensures inspection readiness for risk assessment and centralized monitoring scope

• Ensures adherence to the budget and escalates issues appropriately when needed

• Participates as required in bid defense meetings, sponsor meetings, audits, and other third‑party meetings

• Presents at Risk Manager Forum meetings

• Supports the development of departmental strategies and…