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Data Management

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Descriptif :

ICON plc is a global provider of drug development solutions and services to the pharmaceutical, biotechnology and medical device industries. The company specialises in the strategic development, management and analysis of programs that support clinical development - from compound selection to Phase I-IV clinical studies. With headquarters in Dublin, Ireland, ICON currently, operates from 83 locations in 38 countries and has approximately 14,000 employees. Further information is available at We currently have an exciting opportunity to join our expanding data management team based in one of our many key hub locations across EMEA. .

As the Clinical Data Lead you will be responsible for:
• Point of contact for day to day activity on the study with key responsibilities for study set-up and close-out tasks as well as overseeing and coordinating tasks delegated to the study team.
• Driving the data management teams, studies and programs of studies and independently oversee the performance of data management activities on multiple studies.
• Independently prepare all materials and take part in study kick off meetings.
• Read, ensure understand ing and adhere to the study protocol, contract and scope of work for all task during set-up, maintenance and close-out of the study.
• Set up and maintain data management study files for inclusion in the Trial Master File, ensuring these are maintained in an audit ready state for review by Sponsor, Regulatory or ICON Auditors.

To apply for this role you will need:
• Solid experience in clinical data management experience including proven experience as a data management lead. Key responsibilities for study set-up and close-out tasks as well as overseeing and coordinating tasks delegated to the study team members.
• Experience of at least one of ICON preferred CDMS (e.g. Rave, Oracle Clinical, OCRDC, UX EDC)
• Highly computer literate, including strong Microsoft Office skills (Excel, Word, PowerPoint, Project).
• Excellent communication and interpersonal skills, both verbal and written skills and fluency in your local language and the ability to write and speak English as you will be working in a global team.
• Strong client relationship management skills and the aptitude to develop this further.
• Excellent organizational and planning skills as well as a demonstrated aptitude for project management, and the ability to lead more than one project and prioritize accordingly.

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.

We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.

What’s Next?

Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.

ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment.
Please send your CV to

Contact :

ICON Clinical Research
20 rue Troyon
92316 Sèvres Cédex

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