- Taking leadership of the statistical programming activities
- Creating analysis datasets, tables, listing and figures from clinical trial data
- Develop and validate analysis and reporting deliverables on the safety and efficacy side of programming
- Collaborate effectively with an international team of programmers.
Required Skills and Qualifications:
- BSc in Computer Science, Applied Mathematics, Life Sciences or related fields;
- Minimum 3 years of statistical programming in clinical trials - ideally in safety and efficacy + Leading Project.
- Extended SAS Programming skills, including MACRO, Graphs, and TFLs - tables, figures and listings
- Solid knowledge of the drug development cycle and related guidelines
- Strong analytical mid-set with a particular focus on details
- CDISC experience would be a massive advantage
- Excellent communication skills in English, both verbal and written
Do not hesitate to apply or contact me for more details about this role to:
Yanick Millet
Associate Consultant - Life Sciences Recruitment
Biometrics - SAS Programming, Biostatistics
Tel: +44 (0) 207 255 66 00
yanick.millet@secpharma.com
