Jde Enterpriseone Erp Developer - Latam (Hybrid)

Adecco Colombia S A; Cundinamarca; Híbrido; COP 293.026.000 - 423.260.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible working hours

Onboarding and training options

Health benefits

Career coaching and development

Descripción de la vacante

IQVIA seeks a Centralized Monitoring Lead for LATAM to drive oversight of clinical deliverables across global projects. This role involves coordinating a cross-functional team, maintaining study analytics, and ensuring compliance with ICH GCP and local regulations.

The position is hybrid, based in Colombia, with remote flexibility. The ideal candidate has 3+ years in clinical monitoring, 2+ years in a lead role, and strong English communication.

Formación

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (remote or on-site).
• +2 years in a Lead role.
• Strong written and verbal English (Mandatory).
• Strong organizational, problem solving and decision making skills.
• Excellent motivational, influencing, negotiating and coaching skills.

Responsabilidades

• Lead Centralized Monitoring team and oversee clinical deliverables per protocol and SOPs.
• Act as Clinical Lead when needed and manage IP for studies.
• Manage project resources including CRAs and monitors.
• Trend study metrics and develop action plans.
• Contribute to analytics strategy and advanced analytics initiatives.
• Support monitoring strategy development and triggers/thresholds.
• Attend study team and client meetings.
• Document tools and templates; keep the project audit ready.
• Mentor junior staff.

Conocimientos

Leadership

Communication

English

Organization

Problem solving

Decision making

Coaching

Team management

Educación

Bachelor's degree in life sciences or related field

Herramientas

JD Edwards EnterpriseOne

Power BI

JIRA

Descripción del empleo

Centralized Monitoring Lead in LATAM (Remote)

Buenos Aires, Argentina, Mexico City, Mexico, Santiago, Chile, Lima, Peru, São Paulo, Brazil, Bogota, Colombia

Full time

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Job Overview

The Leader of the Centralized Monitoring team, partner with the project and clinical lead to achieve the delivery of the project's overall objectives to the sponsor's satisfaction per contract, while optimizing speed, quality and cost of delivery and in accordance with IQVIA SOPs, policies and practices.

Essential Functions

• Leadership activities:
• Leader of the Centralized Monitoring team, partner with the project and clinical lead to perform oversight on clinical deliverables on global assigned projects as per the protocol, SOPs, respective regulation/guidelines and project Clinical Operations Plan.
• Unblinded Clinical Lead, including IP management for the assigned study to identify risk and proposed mitigation (including re-supply, re-labelling, Import/export licenses etc.)
• May act as Clinical Lead when there is not assigned to the study and at project close out.
• Manage project resources (CRAs/ Central Monitors/ Clinical Trial Assistants/ Centralized Monitoring Assistants)
• Analytical activities:
• Manage, monitor and complete study/site metrics trending (trend analysis of clinical aspects of the trial, share trends and agree on action plan, review, triage and action clinical study alerts, monitor clinical operation plan compliance etc.).
• Contribute to developing the study specific analytics strategy and work on developing advanced analytics.
• Support project management team to develop monitoring strategy, including monitoring triggers/thresholds.
• Attend study team and /or client meetings.
• Provide Inputs to clinical study teams, key decision makers, and internal team members to manage continuous process improvements, issue escalation, workload projections.
• Development and use of study management plans, and/or RBM specific tools and templates, and/or other study specific plans to evaluate the quality and integrity of the study.
• Ensure complete and accurate documentation of all the study specific tools and templates and keep the project Audit ready, including eTMF oversight.
• Mentors or coaches for junior staff.

Qualifications

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (as remote or on site CRA). Advanced knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements; i.e., ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct.
• +2 years in a Lead role.
• Strong written and verbal communication skills including advanced command of English (Mandatory).
• Strong organizational, problem solving and decision making skills.
• Results and detail-oriented approach to work delivery and output.
• Excellent motivational, influencing, negotiating and coaching skills.
• Ability to work on multiple global projects and manage competing priorities.
• To lead team and effectively work in team.

EEO Minorities/Females/Protected Veterans/Disabled

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 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.

Imagine yourself.

• Thriving in a supportive team environment that inspires you to strive for excellence.
• Joining a companywith a proven track record of success and an exciting future.
• Contributing to a brighter, more sustainable future.

It's possible with a role at ChemTreat ( .

ChemTreat, a Veralto ( company, is the nation's largest and fastest-growing specialty chemical company dedicated solely to industrial water treatment.

When you join the ChemTreat team and the broader Veralto network, you'll have the chance to shape the future of our planet and the future of your career. You'll have opportunities to build new skills and invest in your development, all while doing meaningful work that makes an everyday impact on the world's vital water resources.

Learn more about how our team is maximizing the power of water: offer:

• Flexible working hours
• Professional onboarding and training options
• Powerful team looking forward to working with you
• Career coaching and development opportunities
• Health benefits

Reporting to the **IT Manager, Latin America** , the **JD Edwards EnterpriseOne Developer** is responsible for designing, developing, and optimizing ERP solutions that directly support ChemTreat's operations across Latin America. This role plays a key part in ensuring system stability, enabling efficient business processes, and driving ERP standardization initiatives across the region. As a senior technical contributor, you will influence solution design, collaborate with cross‑functional teams, and support critical business cycles such as monthly financial close.

This position is part of the **Latin America IT Team** , located in Tocancipa, Colombia and will be **hybrid** .

In this role, a typical day will look like

• Designing, developing, and enhancing JD Edwards EnterpriseOne applications to improve operational efficiency.
• Providing third‑level support for JDE production issues and leading complex troubleshooting.
• Performing technical analysis, coding, testing, and deployment following SDLC and change‑control standards.
• Supporting monthly financial close activities in partnership with Finance and Accounting.
• Documenting system changes, configurations, and development work with clarity and accuracy.
• Participating in ERP standardization initiatives across the region.
• Supporting Power BI queries and integrations related to JDE.
• Coordinating and supporting JIRA-based requests for Colombia.
• Collaborating with internal teams and external vendors to resolve technical challenges.

The essential requirements of the job include

• Fluency in English (written and spoken) is required.
• Bachelor's degree in Information Systems, Computer Science, or related field (or equivalent experience)
• 3+ years of ERP experience with strong hands‑on JD Edwards EnterpriseOne development and support
• Experience delivering end‑to‑end JDE solutions in a production environment
• Experience supporting integrations, reporting, and analytics (Power BI preferred)

Unsolicited Assistance

We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at any of the Veralto companies ( , in any form without a valid, signed search agreement in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Veralto and its companies. No fee will be paid in the event the candidate is hired by Veralto and its companies because of the unsolicited referral.

Veralto and all Veralto Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.

ChemTreat is proud to be a part of the Water Quality segment of Veralto (NYSE: VLTO), a $5B global leader dedicated to ensuring access to clean water, safe food and medicine, and trusted essential goods.

At Veralto, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.