IQVIA
Project Management Analyst (Remote)
Project Management Analyst | IQVIA | Worldwide
Job Overview
Project Management Analysts (PMA) are an integral part of clinical trialdelivery, liaising with clinical teams to improve patients’ lives bybringing new drugs to the market faster. The PMA works in partnership withthe Project Leader (PL)/Clinical Project Manager (CPM) providing supportwith project management activities to mitigate risk, control cost, manage...
Project Management Analyst | IQVIA | Worldwide
Job Overview
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. Experience with ARIBA required.
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.
Qualifications
Bachelor’s Degree Life sciences or other related field Req
Typically requires 2 years of prior relevant experience.
- Requires knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education.
- 1 year of relevant clinical research experience with analytical/financial skills or relevant Project Management experience or equivalent combination of education, training, and experience.
- Knowledge of clinical trials – knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements i.e. International Conference on Harmonization (ICH), Good Clinical Practice (GCP), relevant local laws, regulations, and guidelines, towards clinical trial conduct.
- Communication – strong written and verbal communication skills including good command of English language.
- Problem solving – problem solving skills.
- Organization – planning, time management and prioritization skills.
- Prioritization – ability to handle conflicting priorities.
- Quality – attention to detail and accuracy in work.
- Results-oriented approach to work delivery and output.
- IT skills – good software and computer skills, including Microsoft Office applications, including but not limited to, Microsoft Word, Excel, and PowerPoint.
- Collaboration – ability to establish and maintain effective working relationships with coworkers, managers and clients.
- Cross-collaboration – ability to work across geographies displaying high awareness and understanding of cultural differences.
- Effective communication – ability to influence without authority.
- IQVIA Core Competencies – ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).
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
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