Clinical Data Programming Lead
Talent Acquisition Business Partner
- Full Service Division
About the role
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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
Application process
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