ACUTA
Providing Regulatory Information Management (RIM) solutions and services to the Life Sciences and related industry.
- Open roles
- 40
- New role every
- ~0.1 days
Company signals
Score: 69Job facts
- Location
- Mexico City, Mexico
- Type
- Full-time
- Posted
- May 29, 2026
More roles at ACUTA
- Asistente de Datos Junior · Bogota, Colombia
- Analyst (Consulting) · Mexico City, Mexico
- Clinical Research Coordinator, On-site, Elkhorn, NE · Elkhorn, NE, United States of America
- Site Research Assistant (Rosario) · Buenos Aires, Argentina
- Associate Director, HR · Durham, North Carolina, United States of America
- Regulatory and Start Up Specialist - Portugal · Lisbon, Portugal
Project Management Analyst in Mexico and Argentina
at ACUTA
Project Management Analysts (PMA) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster. The PMA works in partnership with the Project Leader (PL)/Clinical Project Manager (CPM) providing support with project management activities to mitigate risk, control cost, manage project schedule, and ensure customer satisfaction related to assigned project/s.
Essential Functions
• Establish and manage performance dashboards, analyze event triggers/alerts
and determine appropriate follow up for Project Leader (PL) or other
function(s) to act upon.
• Coordinate project schedule and ensure timely updates of all key milestone
and partner with PL on related calls.
• Coordinate and support the risk and issue management process.
• Manage all aspects of the Project Finances including Estimate at Completion
(EAC), monthly expenses, invoices and reconciliation.
• Demonstrate compliance with the Vendor and Purchase Order (PO) Management
process.
• Implement and maintain baseline and change control processes.
• Ensure PL has timely and accurate data on areas including cost, schedule,
scope, utilization, change orders and quality to support better decision-
making.
• Develop and maintain relevant sections of Project Management Plans.
• Review and support project resource allocation within project budgeted for
assigned portfolio/ projects.
• Prepare correspondence, including meeting minutes, for project team and/or
customer.
• Organize and partner with PL in managing internal project team and customer
meetings.
• Prepare project status reports and presentation materials for internal
project team and customer meetings.
• Manage and coordinate core file reviews and support audits as needed. Drive
e Trial Master File (eTMF) filing compliance focusing on completeness,
timeliness and quality.
• Manage project specific eTraining and oversee compliance.
• Coordinate and support onboarding of new Key Project Team Members and system
access.
• Monitor project metrics and make required updates in IQVIA systems to ensure
accurate and timely reporting is available to senior management.
• Participate in regional initiatives to support Project Management Analyst
(PMA) community and aid personal development.
Qualifications
• Bachelor's Degree Life sciences or other related field.
• Typically requires +2 years of prior relevant experience.
• Requires knowledge of principles, theories, and concepts of a job area,
typically obtained through advanced education.
• Ideally, 1 year of relevant clinical research experience with
analytical/financial skills or relevant Project Management experience or
equivalent combination of education, training, and experience. Also, previous
background in a consulting company is really useful.
• Advanced level of English is mandatory , due to daily use
LI-NRJ #LI-Remote
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.