Service Supervisor

Cummins Latin America; San Juan; A distancia; ARS 137.157.000 - 198.116.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Connectivity allowance

Gym reimbursement

PedidosYa credit

Statutory vacation

Health insurance

Descripción de la vacante

IQVIA is seeking a Centralized Monitoring Lead in LATAM for a 100% remote, full-time role. You will partner with project and clinical leads to deliver high-quality clinical monitoring while optimizing speed, quality and cost, following IQVIA SOPs.

You will oversee analytical work, manage resources, and mentor staff across global projects, while ensuring compliant documentation and robust risk management.

Formación

• Bachelor's degree in life sciences or related field.
• +3 years of relevant clinical monitoring experience (remote or on-site CRA).
• +2 years in a Lead role.

Responsabilidades

• Lead the Centralized Monitoring team and oversee global projects.
• Provide IP management and risk mitigation strategies.
• Mentor junior staff and drive process improvements.
• Manage study resources and monitoring activities across sites.
• Ensure documentation and RBM tools are audit-ready.

Conocimientos

Leadership

Communication

Project coordination

Educación

Bachelor's degree in life sciences or related field

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.

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.

EEO Minorities/Females/Protected Veterans/Disabled

100% Remote Full-time

English: Intermediate/Advanced (required — interviews conducted in English) | 9:00 AM – 5:00 PM UTC

CVs must be submitted in English

About the Role

Join the team supporting one of the world's largest automotive manufacturers, working within a global consulting firm to lead the planning and execution of a critical data migration program. You will coordinate cross-functional teams, define the migration approach and controls, and manage risks to ensure a smooth and reliable transition to the target system.

Responsibilities

Lead the end-to-end planning and execution of data migration activities

Ensure data is accurate, complete, and ready for use in the target system

Coordinate cross-functional migration teams across workstreams

Define the data migration approach, methodology and quality controls

Identify, assess and manage migration risks and issues

Ensure a smooth and reliable transition with minimal disruption

Report migration status and progress to senior stakeholders

Required Skills

Proven experience as a Data Migration Lead or Team Lead in large-scale enterprise programs

Strong knowledge of data migration methodology : extraction, transformation, cleansing, validation and loading

Experience coordinating cross-functional teams across multiple workstreams

Ability to define migration controls and risk management strategies

Experience working in S/4HANA or similar ERP migration programs (preferred)

Intermediate to advanced English — interviews and daily work conducted in English

Availability to work in UTC timezone (9:00 AM – 5:00 PM)

Hiring Process

• Collaborative environment with high-impact projects across leading industries
• Connectivity allowance
• Gym reimbursement
• PedidosYa credit
• Statutory vacation
• Health insurance: Swiss Medical or OSDE