Associate Manager, Statistical Programming

The Associate Manager, Statistical Programming is responsible for the statistical programming aspects of projects for clients and project teams through taking the lead on studies, assisting teams in meeting deadlines by taking part in programming activities, management of internal staff and/or for 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.

What we do

For more than 27 years, Veristat has built a reputation as global experts in clinical development.

• 760+ Rare Disease Clinical Trials supported
• 160+ Marketing Applications supported
• In 2022 we supported 8 marketing applications that received regulatory approval
• Learn more about our core values here!

What we offer

• The estimated hiring range for this role is £50-70K GBP plus applicable bonus. This hiring range is specific to United Kingdom and will vary for other regions based upon local market data.  Final salary is ultimately decided upon taking into account a wide range of factors, including but not limited to: skills and experience, licensure and certifications, education, specific location and dynamic market data.

• Benefits vary by location and may include:
  • Remote working
  • Flexible time off
  • Paid holidays
  • Medical insurance
  • Tuition reimbursement
  • Retirement plans

What we look for

• 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 knowledge of regulatory requirements and drug development process.
• Excellent organizational skills and verbal/written communication skills.
• Strong communication skill set with peers, business partners, and Sponsors.
• Strong analytical mindset.