Job Description

Job Category: Statistical Programming - FSP
:
Sponsor-dedicated:
Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership.
Position Overview:
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills to support one or more Phase I-IV clinical trials, with a focus on Oncology.
Our values

• We believe in applying scientific rigor to reveal the full promise inherent in data.
• We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
• We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
• We prize innovation and seek intelligent solutions using leading-edge technology.

Responsibilities:
How you will contribute:

• Performing data manipulation, analysis and reporting of clinical trial data on both safety and efficacy, utilizing SAS programming.
• Applying CDISC know-how and proficiency to create and validate ADaM datasets/analysis files as well as tables, listings, and figures (TLFs).
• Applying your strong understanding/experience with safety and efficacy analyses.
• Generating complex ad-hoc reports.
• Preparing and validating submission packages, i.e. define.xml, Reviewers Guides, Pinnacle 21 reports.
• Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
• Being adaptable and flexible when priorities change.

Qualifications:
Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
At least 5 years of relevant statistical programming experience in a clinical development environment with 3 years of efficacy preferred.
BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences, or other related scientific subjects.
Excellent SAS data manipulation, analysis, and reporting skills. * Ability to implement the latest CDISC ADaM standards (production/validation).

• Strong understanding/experience with ADaM efficacy dataset development is required.

Experience with Oncology is required.
Experience with submission packages is a plus
Working knowledge of latest CDISC SDTM standards.
Very good oral and written English communication skills.

Skills Required