Clinical Data Programming Lead

Clinical Data Programming Lead

Key responsibilities include:

• Planning and working with the clinical programming group to schedule specification, programming, validation and ongoing delivery activities.
• Ability to write and execute SAS programs to produce internal and Sponsor deliverables.
• Leads timelines for programming setup process, ensuring issues are addressed and producing clinical data delivery validation packages to the study teams to file in the Trial Master File.
• Participates in activities related to the specification review, program validation and quality assurance of study data deliverables, applying expert experience and knowledge to support the clinical data programmers assigned to a clinical study.
• Attends sponsor audits, including presenting the Clinical Data Delivery process and procedures from a compliance perspective.

To succeed you will need:

• Degree in a Technical or Science background coupled with strong experience in Clinical Data Management and SAS programming.
• Ability to work to tight deadlines and effectively run multiple projects to specific client requests
• Strong communication skills as you will be working across a highly matrix organisation internally and externally.

Benefits of Working in ICON