Remote Clinical Project Management Analyst

IQVIA Inc

Buenos Aires

Remote

ARS 92,909,000 - 139,364,000

Full time

8 days ago

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Job summary

IQVIA Inc is seeking a Project Management Analyst (PMA) to support clinical trial delivery by working with clinical teams and the Project Leader. You will help mitigate risk, control costs, manage schedules, and ensure customer satisfaction for assigned projects.

The role emphasizes dashboard development, milestone tracking, and efficient collaboration with cross-functional teams globally. Advanced English is mandatory and prior clinical research exposure is advantageous.

Qualifications

  • Bachelor's Degree Life sciences or related field.
  • Typically requires +2 years of prior relevant experience.
  • Ideally 1 year of clinical research experience with analytical/financial skills or PM experience; consulting background helpful.
  • Advanced English is mandatory due to daily use.

Responsibilities

  • Establish and manage performance dashboards and analyze events and triggers.
  • Coordinate project schedules and milestone updates with the Project Leader.
  • Support risk and issue management processes.
  • Manage project finances including EAC, expenses, invoices and reconciliation.
  • Ensure data in IQVIA systems supports timely senior management reporting.
  • Prepare status reports and meeting materials for teams and customers.
  • Assist onboarding of new team members and system access.

Skills

Project management
Analytical skills
Financial skills
Communication
English proficiency

Education

Bachelor's degree Life sciences

Job description

IQVIA Inc is seeking a Project Management Analyst (PMA) to support clinical trial delivery by working with clinical teams and the Project Leader. You will help mitigate risk, control costs, manage schedules, and ensure customer satisfaction for assigned projects.

The role emphasizes dashboard development, milestone tracking, and efficient collaboration with cross-functional teams globally. Advanced English is mandatory and prior clinical research exposure is advantageous.

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