Senior Statistical Programmer

JR United Kingdom; Greater London; Hybrid; GBP 50,000 - 90,000; Full time

Job summary

An international CRO is seeking a Freelance Senior Statistical Programmer to join their team for a contract role focused on rare diseases. This position offers the opportunity to work on critical clinical trial data, including data manipulation, analysis, and reporting. The ideal candidate will have extensive SAS programming experience and a strong background in clinical trials. With the flexibility of remote work and the requirement of just one day on-site in Central London, this role is perfect for professionals looking to make an impact in the healthcare sector. Join a dynamic team and contribute to innovative solutions in rare disease research.

Qualifications

• Extensive experience with SAS Programming within clinical trials.
• Strong knowledge of CDISC, ADaM, and SDTM standards.

Responsibilities

• Perform data manipulation, analysis, and reporting of clinical trial data.
• Create SDTM and analysis data sets, and generate TLGs.

Skills

SAS Programming

Data Manipulation

Clinical Trial Data Analysis

Ad-hoc Analysis

System-level Macro Programs

Education

Life Science Degree

Tools

SAS/GRAPH

CDISC

ADaM

SDTM

Job description

We are currently partnered with an international CRO that is looking for a Freelance Senior Statistical Programmer to work FSP to a Rare Disease pharma.

This position is offered on a contract, outside of IR35 until the end of the year, with a very high likelihood of extending. One day per week required on-site in Central London. Available to start ASAP.

Candidate must be based in the UK.

Responsibilities:

• Perform data manipulation, analysis and reporting of primarily clinical trial data;
• Create SDTM data sets;
• Create analysis data sets;
• Program and generate tables, listings and graphs (TLGs);
• Validate and document SAS programs and output;
• Fulfill ad-hoc analysis requests;
• Other services as identified by client.

Requirements:

• Life Science degree or equivalent;
• Extensive experience with SAS Programming within clinical trials;
• Strong knowledge and experience with CDISC, ADaM and SDTM;
• Previous experience leading studies;
• Rare Disease experience is an advantage;
• Expertise in the development and use of system-level macro programs;
• Experience in programming using SAS/GRAPH.

For more information, please get in contact with Jack Kavanagh at AL Solutions.