Statistical Programmer I FSP

Cytel; Columbia (SC); On-site; USD 70,000 - 90,000; Full time

Job summary

Cytel invites recent graduates to join a sponsor-dedicated Statistical Programmer program embedded with one of our pharmaceutical clients, delivering data-driven insights with autonomy and ownership. You will apply SAS programming to support Phase I–IV trials, manipulating and reporting safety and efficacy data, and preparing submission-ready datasets and listings.

Cytel provides training and cross-functional collaboration in a globally dispersed team, with emphasis on clear English

Qualifications

• Minimum 4 years of Undergraduate study plus 2 years of Graduate-level education.
• Academic training in Statistics, Epidemiology, or Data Science; and Computer Science, Mathematics, or Computational Science.
• Foundational data manipulation, analysis and reporting skills; strong English communication; ability to work in a globally dispersed team.

Responsibilities

• Perform data manipulation, analysis, and reporting of clinical trial data using SAS programming.
• Create and validate datasets, analysis files, tables, listings, and figures (TLFs) for submissions.
• Generate ad-hoc reports and prepare submission packages.
• Work effectively in a globally dispersed team and adapt to changing priorities.

Skills

Team collaboration

English communication

Analytical mindset

Education

Statistics or Data Science

Computer Science or Mathematics

Tools

SAS programming

Job description

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:

We are looking for a Recent Graduate to perform and act as a Statistical Programmer, where you will leverage your education to develop and expand programming skills, supporting one or more Phase I-IV clinical trials. This is a great opportunity to start a career in Clinical Life Sciences, supported by Cytel and embedded in a trusted partner.

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
• Applying your SAS programming skills, to create and validate datasets/analysis files, tables, listings, and figures ( TLF s)
• Generating ad-hoc reports
• Preparing and validating submission packages
• Applying your understanding/experience with Efficacy analysis
• 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

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:

• A minimum of 4 years of Undergraduate study and 2 additional years of Graduate-level education
• Academic training in both of the following 2 categories (or closely related fields)
• Statistics, Epidemiology, or Data Science
• Computer Science, Mathematics, or Computational Science
• Foundational data manipulation, analysis and reporting skills
• Familiarity with drug development life cycle and a passion to learn and expand knowledge
• 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 learn and perform statistical programming and related tasks

Cytel Inc. is an Equal Employment / Aff ...