Senior Statistical Programmer FSP

TREIZE-QUARANTE (1340); London; Remote; GBP 60,000 - 100,000; Full time

Job summary

An innovative firm is seeking a Senior Statistical Programmer to join their dynamic team, supporting cutting-edge clinical trials. In this role, you will leverage your advanced SAS programming skills and expertise in CDISC standards to drive the analysis and reporting of clinical trial data. You will work closely with cross-functional teams, ensuring high-quality deliverables while navigating the complexities of the pharmaceutical industry. This position offers the flexibility of remote work, allowing you to contribute to impactful projects that enhance patient treatment across various therapeutic areas. If you're passionate about data and eager to make a difference, this opportunity is for you.

Qualifications

• 8+ years of SAS programming experience in clinical trials.
• Strong knowledge of CDISC SDTM/ADaM standards.

Responsibilities

• Perform data manipulation and analysis of clinical trial data.
• Generate and validate SDTM and ADaM datasets.

Skills

SAS Programming

Data Manipulation

CDISC Standards

Efficacy Analysis

QC / Validation Skills

Ad-hoc Reporting

Analytical Skills

Troubleshooting Skills

Education

Bachelor’s Degree in Statistics

Master’s Degree in Statistics

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

Position Overview:

As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.

How you will contribute:

• Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming
• Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs)
• Production and QC / validation programming
• Generating complex ad-hoc reports utilizing raw data
• Applying strong understanding/experience of Efficacy analysis
• Creating and reviewing submission documents and eCRTs
• 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

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 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.
• Study lead experience, preferably juggling multiple projects simultaneously preferred.
• Strong SAS data manipulation, analysis and reporting skills.
• Solid experience implementing the latest CDISC SDTM / 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.
• Submissions experience utilizing define.xml and other submission documents.
• Experience supporting immunology, respiratory or oncology studies would be a plus.
• Excellent analytical & troubleshooting skills.
• Ability to provide quality output and deliverables, in adherence with challenging timelines.
• Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.