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Project Management Analyst

Employer
IQVIA
Location
Sofia
Start date
30 Nov 2021
Closing date
30 Dec 2021

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Discipline
Project Management, Clinical Project Management
Hours
Full Time
Contract Type
Permanent
Experience Level
Graduate

Job Details

Our Project Management Analysts (PMA's) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients’ lives by bringing new drugs to the market faster.

As a PMA you will work in partnership with the Project Leader/ Clinical Project Manager in one of our therapeutic areas including Internal Medicine, Central Nervous System, Immunology & Women’s Heath, Cardiovascular Renal Metabolic, Early Clinical Development, Oncology or Gastroenterology. Your key purpose will be to support with project management activities to mitigate risk, control cost, manage project schedule, and ensure customer satisfaction related to assigned projects.

Essential Functions

  • Establish and manage performance dashboards, analyse event triggers/alerts and determine appropriate follow up for Project Leader or other functions

  • Coordinate project schedule and ensure timely updates of all key milestone and partner with Project Leader 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 Project Leader 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, project status reports and presentation materials for 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

Qualifications and Experience Required

  • Bachelor's Degree in Life Sciences or other related field, typically with up to 2 years of prior relevant experience

  • 1 year of relevant clinical research experience with analytical/financial skills or relevant Project Management experience or equivalent combination of education, training, and experience

  • Strong written and verbal communication skills including good command of English language

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

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