Clinical Data Lead

Key Responsibilities & Duties:

1. To act as key point of contact for the sponsor and the study team on day to day study data issues, e CRF design, edit checks and other implemented documents.
2. To take part in study kick off (internal and external) meeting with DMPM
3. To identify out of scope tasks and bring to the attention of DMPM and contract analyst
4. To develop an understanding of the revenue recognition and revenue forecasting process and assist the DMPM on a monthly basis.
5. To lead the development of specifications, implementation and testing of the CRFs, edit checks and data review and oversight listings (DVS)
6. To lead the development of DMP and study specific procedures and assisting DMPM in development of project plan and timelines.
7. To set up and maintain data management study files for inclusion in the Trail Master file and ensuring these are maintained in audit ready state.
8. He/ She should possess excellent organizational and planning skills as well as a demonstrated aptitude or project management and ability to lead more than one project and prioritize accordingly.

1. A minimum of 7 years clinical data management or other relevant experience Currently
2. Working as a Team Lead/ Associate Data Lead
3. Experience of at least one of ICON preferred CDMS (Rave, Inform, Oracle Clinical, OCRDC)
4. Highly computer literate, including strong Microsoft Office skills (Excel, Word, PowerPoint, Project)
5.  Strong client relationship management skills, and the aptitude to develop this further