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.
We have an fantastic opportunity for a Project Manager, Data Management to join ICON.
The DMPM role in the Early Phase Data Management department is responsible for managing data management teams, studies and programs of studies under the general direction of the Senior Manager/Director of Data Management. Provide planning estimates for project scope, schedule, and resource requirements and ensuring that studies are properly managed and delivered. Work with Clinical Operations, Biostatistics, SAS Programming, Medical Writing and Quality Assurance to ensure that data collected during trials are managed according to corporate standards and meet regulatory guidelines for data integrity.
The Early Phase service line of the company specializes in the strategic development, management and analysis of studies and programs that support Phase 1/2a clinical development.
Location
Europe - Home based role
About the DMPM role within ICON
The DMPM role will manage a number of fast moving early phase studies or programs of studies to ensure project objectives are met within budget, to agreed timeline and to high level of quality. You will manage a global team of clinical data management resources. The DMPM will provide input into CRF design, protocol review, edit check specifications, data entry conventions, monitoring guidelines, and any other study related documents and be responsible for the maintenance, cleaning and lock of the EDC study databases. Must have a minimum of 8 years clinical data management experience and a minimum of 3 years study lead experience.
To succeed you will need
You will need a minimum of 8 years clinical data management experience. Bachelor's degree in a scientific discipline. Experience with at least one of ICON preferred CDMS (Rave, Inform, Medrio, OCRDC).
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 through the form below.
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