Senior Statistical Programming Lead, EU Clinical Trials

1 month ago


London, Greater London, United Kingdom Lifelancer Full time

**Company Overview:**

At Lifelancer, we are a talent-hiring platform in Life Sciences, Pharma and IT, connecting professionals with opportunities in pharma, biotech, health sciences, healthtech and IT domains.

**Salary & Benefits:**

We offer a highly competitive salary ranging from £50,000 to £70,000 per annum, plus applicable bonus, depending on skills, experience, education, and location. Our benefits package includes remote working, flexible time off, paid holidays, medical insurance, tuition reimbursement, and retirement plans.

**Job Description:**

The Senior Statistical Programming Lead will take the lead on statistical programming aspects of projects for clients and project teams. This role involves managing internal staff, maintaining optimal department processes, implementing project-specific strategies, and assisting with the development and implementation of department strategies to increase productivity and quality while decreasing cycle times and costs.

**Required Skills & Qualifications:**

To succeed in this role, you will need:

  • A Master's degree in technology, statistics, pharmaceutics or another related science or mathematics field with a minimum of 5 years of SAS programming experience with clinical trial data using CDISC SDTM and ADaM implementation guidelines OR Bachelor's with a minimum of 8 years of SAS programming experience with clinical trial data using CDISC SDTM and ADaM implementation guidelines.
  • 1 year of supervisory OR 2 years of project lead experience in a CRO required.
  • Excellent working knowledge of CDISC SDTM and ADaM Implementation Guidelines.
  • Thorough knowledge of International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines and other applicable regulatory rules and guidelines as well as of medical terminology, clinical trials, and clinical research.
  • Working knowledge of the relationship and regulatory obligation of the contract research organization (CRO) industry with pharmaceutical and biotech companies.
  • Excellent organizational skills and verbal/written communication skills.
  • Strong analytical mindset.


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