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Sr. Project Management Analyst

IQVIA -
Buenos Aires, Buenos Aires

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Detalles del empleo

Tiempo completo
Hace 2 horas

Descripción completa del empleo

Buenos Aires, Argentina | Full time | Home-based | R1559187

**Please submit your resume in English**

As a Senior Project Management Analyst (Sr. PMA), you will play a key role in the successful delivery of global clinical trials by partnering closely with Clinical Project Managers and cross-functional study teams.

This is an exciting opportunity for a detail-oriented, analytical, and collaborative professional who enjoys combining project management, financial oversight, process improvement, and operational excellence. You will contribute directly to the planning, execution, and governance of clinical research projects, helping ensure studies are delivered on time, within budget, and in compliance with quality and regulatory standards.

What You'll Do

Partner with Clinical Project Managers and Project Leaders to support the successful delivery of global clinical trials.
Maintain project plans, study timelines, milestones, and performance dashboards to ensure accurate project tracking and reporting.
Lead project risk and issue management activities, driving mitigation strategies and process improvements.
Manage project financials, including forecasting, budgets, invoicing, reconciliation, and change order processes.
Support vendor oversight, resource planning, and project governance activities.
Drive TMF/eTMF quality and compliance, supporting audits, inspections, and training requirements.
Prepare project reports, presentations, and key operational insights to support decision-making.
Mentor junior PMAs and contribute to initiatives that enhance project management best practices.

Required Qualifications

Bachelor's degree in Life Sciences, Health Sciences, Business, or a related field.
3+ years of experience in clinical research, clinical operations, project management, or a related field.
Knowledge of clinical trial processes and regulatory requirements, including ICH-GCP and applicable local regulations.
Advanced written and verbal communication skills in English.
This is a fully remote position.

Preferred Qualifications

Experience working within a CRO, pharmaceutical, biotechnology, or healthcare environment.
Knowledge of project management methodologies and tools.
Experience with eTMF, CTMS, financial systems, and clinical trial technologies.
Experience supporting global and cross-functional teams.

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.

Where you'll work

Home-based

You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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