Senior Project Manager
- India
- Project Management
- ICON Strategic Solutions
- Remote
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About the role
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ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
[Project Manager]
[India]
PM has responsibility for one or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies.
The PM leads and manages the tactical execution of one or more clinical studies from study startup through database release.
The PM provides quality oversight to the Contract Research Organization (CRO) and of the CRO deliverables related to study execution.
The PM leads and coordinates the execution of a clinical trial from Study start-up through Database release and inspection readiness to ensure timely delivery of quality study data. Study Managers may also provide input to support compilation of sections to Clinical Study Reports.
The PM will provide leadership to the teams in the setting of realistic recruitment targets and delivery milestones as the single point of accountability for detailed study start-up and monitoring plans and for delivery to the agreed plans.
The PM is a core member of the Study Team and will represent the CRO on matters of study execution.
The PM works with functional lines and directly with CRO line functions to resolve or triage site level issues.
The PM will drive decision making and work closely with the Clinical Study Team Lead to provide input to operational strategy.
- At least 10 yrs overall clinical research experience
- Must have at least 2 years regional/global PM experience
- High priority of vendor & CRO management experience preferred
- Fluent English
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
Application process
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Reasonable AccomodationsDay in the life

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Career ProgressionContent type
BlogsPublish date
05/30/2023
Summary
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04/21/2023
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From Clinical Trial Assistant to Clinical Operations Manager, Adrienne Purdy shares her journey.Tell us about you role and what you do at ICON? I have been at ICON since 2013 and I have been growing
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11/05/2014
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