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Principal Statistical Programmer FSP

Cytelleón, España

Hace 9 días

Descripción del trabajo

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JOB DESCRIPTION

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 Principal Statistical Programmer (or, depending on your level and experience, Principal 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.

Sponsor-dedicated

JOB DESCRIPTION

Position Overview

As a Principal Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (ADaM and TFL) to support programming on the basis of clinical study and project data. You will be assigned to our client's programming team with a responsibility for publication analyses, HTA-related data reanalysis, adhoc analyses and other challenging activities. This role can be performed as fully remote.

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 programming of datasets and outputs based on customer internal requests, using predominantly SAS, in an environment that requires flexibility and independence.

Generating and validating ADaM datasets / analysis files, and tables, listings, and figures (TLFs) for clinical studies in phase 1-4 and potentially for pooled analyses (like ISS / ISE)

Production and QC / validation programming

Generating complex ad-hoc reports utilizing raw data

Applying strong understanding / experience of Efficacy analysis

Creating and reviewing related documents

Communicating with and / or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries

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

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 :

Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.

At least 6 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 4 years of related experience with a master’s degree or above. Knowledge of early phase / PK / PD could be a plus.

Strong SAS data manipulation, analysis and reporting skill. R knowledge is a plus.

Solid experience implementing the latest CDISC ADaM standards.

Strong QC / validation skills.

Good ad-hoc reporting skills.

Proficiency in Efficacy analysis.

Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.

Experience supporting neuroscience or immunotherapy projects would be a plus.

Excellent analytical & troubleshooting skills.

Ability to provide quality output and deliverables, in adherence with challenging timelines.

Flexible, independent mindset; self-organized and a good communicator and team player.

Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Seniority level

Seniority level Mid-Senior level

Employment type

Employment type Full-time

Job function

Job function Research, Analyst, and Information Technology

Industries Pharmaceutical Manufacturing

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