Statistical Programmer Ii 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 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. This is an exciting time to be a part of this new program.

**Position Overview**:

- As a Statistical Programmer, you will leverage your advanced SAS programming skills to support or lead one or more Phase I-IV clinical trials.

ShortDescriptionStr

Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity come together to advance the state of clinical development.

**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 4+ years of relevant experience in statistical programming in the clinical development environment
- Excellent SAS data manipulation, analysis and reporting skills
- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
- Excellent oral and written English communication skills
- Ability to provide quality output and deliverables, in adherence with challenging timelines
- Willingness and ability to learn and follow Company’s standard processes and procedures.
- Ability to effectively perform complex statistical programming and related tasksWillingness and ability to provide guidance to team members on technical and process questions

**Preferred Qualifications**:

- In-depth knowledge of SAS Graph and other SAS Statistical packages
- Prior publication work experience

InternalQualificationsStr

**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 4+ years of relevant experience in statistical programming in the clinical development environment
- Excellent SAS data manipulation, analysis and reporting skills
- Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
- Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners
- Excellent oral and written English communication skills
- Ability to provide quality output and deliverables, in adherence with challenging timelines
- Willingness and ability to learn and follow Company’s standard processes and procedures.
- Ability to effectively perform complex statistical programming and related tasksWillingness and ability to provide guidance to team members on technical and process questions

**Preferred Qualifications**:

- In-depth knowledge of SAS Graph and other SAS Statistical packages
- Prior publication work experience

InternalResponsibilitiesStr

**As a Statistical Programmer, your responsibilities will include**:

- Performing data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
- Generating complex ad-hoc reports
- Preparing and validating submission packages
- Preparing submission packages
- Performing lead duties when called upon
- 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

ExternalResponsibilitiesStr

**As a Statistical Programmer, your responsibilities will include**:

- Performing data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
- Generating complex ad-hoc reports
- Preparing and validating submission packages
- Preparing submission packages
- Performing lead duties when called upon
- 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