AL2S3 LTD: Freelance Senior Statistical Programmer

Programmer is needed in London, United Kingdom.

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Client: AL2S3 LTD

Location: London, UK

Contract: Full Time, Freelance

Company Introduction

Ashley Smith-Brown is partnered with a dynamic, global pharmaceutical company with a strong presence in the industry. Their client is at the forefront of ground-breaking research, dedicated to improving the lives of millions worldwide through innovative medicines. With a commitment to scientific excellence and a passion for discovering life-changing therapies, this company is driving the future of healthcare.

Job Title: Senior Statistcal Programmer

Are you a seasoned Statistical Programmer, searching for an exciting opportunity to showcase your expertise and make a significant impact? I have a fantastic opportunity just for you!

Job Description

As a Senior Statistical Programmer, you will play a crucial role in the development and analysis of clinical trials, supporting the company’s mission to bring life-saving treatments to patients in need. You will collaborate closely with cross-functional teams, including statisticians, data managers, and clinical researchers, to ensure the highest quality standards are met throughout the clinical development process.

Key Responsibilities

• Utilize your expertise in statistical programming to develop, validate, and maintain analysis datasets, tables, figures, and listings for clinical studies.
• Apply advanced statistical techniques to analyse and interpret data, providing critical insights that contribute to decision-making processes.
• Collaborate with internal stakeholders to ensure programming activities are aligned with project timelines, quality standards, and regulatory requirements.
• Contribute to the development and implementation of innovative programming methodologies, tools, and standards, enhancing overall efficiency and productivity.
• Mentor and guide junior programmers, fostering their professional growth and ensuring adherence to best practices within the team.

Requirements

• Bachelor’s degree in a quantitative field, such as Statistics, Computer Science, or related disciplines.
• Extensive experience in statistical programming within the pharmaceutical industry or a related field.
• Proficiency in programming languages commonly used in clinical research, such as SAS and R.
• Strong understanding of CDISC standards, including SDTM and ADaM.
• Excellent communication and collaboration skills, with the ability to work effectively in cross-functional teams.
• Attention to detail and a commitment to delivering high-quality work in a fast-paced environment.
• Familiarity with regulatory guidelines and industry best practices related to statistical programming.