Project Management Analyst in Mexico and Argentina

IQVIA

Buenos Aires

Teletrabalho

ARS 1 200 000 - 1 800 000

Tempo integral

Há 9 dias

Uma candidatura completa num minuto

Currículo e carta de apresentação personalizados, prontos a enviar.

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Resumo da oferta

IQVIA is seeking a Project Management Analyst to support clinical trial delivery. You will partner with the Project Leader and functional teams to manage schedules, risk, and finances, ensuring timely decisions and high-quality reports.

The role requires 2+ years of relevant experience, strong English, and a background in life sciences or clinical research. Remote-friendly with global collaboration opportunities.

Qualificações

  • Bachelor's degree in Life sciences or related field.
  • Typically requires +2 years of prior relevant experience.
  • Ideally 1 year of relevant clinical research experience with analytical/financial skills or relevant Project Management experience.
  • Previous background in a consulting company is useful.
  • Advanced level of English is mandatory.

Responsabilidades

  • Establish and manage performance dashboards, analyze events and determine follow up for Project Leader or other functions.
  • Coordinate project schedule and ensure timely updates of milestones and partner calls.
  • Coordinate and support risk and issue management processes.
  • Manage all aspects of project finances including EAC, monthly expenses, invoices and reconciliation.
  • Ensure compliance with Vendor and PO management processes.
  • Implement and maintain baseline and change control processes.
  • Provide PL with timely data on cost, schedule, scope, utilization, and quality.
  • Develop and maintain sections of Project Management Plans.
  • Review and support project resource allocation within budget.
  • Prepare correspondence including meeting minutes for team or customer.
  • Organize and partner with PL for internal and customer meetings.
  • Prepare project status reports and presentations.
  • Manage core document reviews and audits; drive eTMF filing compliance.
  • Manage eTraining and oversee compliance.
  • Coordinate onboarding of new Key Project Team Members and system access.
  • Monitor project metrics and update IQVIA systems for timely reporting.
  • Participate in regional initiatives to support PMA community and personal development.

Conhecimentos

Project management
Analytical skills
Financial skills
English (advanced)
Consulting experience

Formação académica

Bachelor's degree in life sciences or related field

Descrição da oferta de emprego

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.

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