Senior Clinical Data Lead

Senior CDL - Wavre, Belgium

Due to an expansion with one of ICON's exciting key clients, we are currently looking to grow our EU Data Management team in Wavre, Belgium. Both organisations join together with a strong science and technology focus to deliver best in class solutions to the healthcare industry.

As the Senior CDL 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, Inform, 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.
• 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.