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- SAS, ISS, ISE, Saftey and Efficacy
- Experience with CDISC, ADaM, and SDTM standards.
- Experience as a Study lead Programmer
- Tables, Listings, and Figures.
- Submission, FDA, SAP
- 6-month and 12-Month Contract (Possibility of Extension)
- Working with Leading Pharma
- Start Date: ASAP.
Contractor Statistical Programmer - United Kingdom - Warman O'Brien
Description
A CRO is looking to hire contract Statistical SAS Programmers at either a Senior or Principal level. You will need to have a good understanding of SAS Programming and worked within the Pharma industry. Therefore you would need to have experience working with ADaM, SDTM, and CDISC standards. The main experience needed includes FDA Submission, ISS, ISE, Safety and Efficiency, Oncology, SAP Specifications, and a proven ability to communicate between internal and external teams.
Details:
If you would like to find out more information about the role and company, please get in touch.