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Clinical Trials Lead Programmer

2 mesi fa

Milano, Lombardia, Italia Thermo Fisher Scientific A tempo pieno
About the Role

We are seeking a highly experienced and motivated Clinical Trials Lead Programmer to join our dynamic team at Thermo Fisher Scientific.

In this role, you will oversee the statistical and programming aspects of multiple projects, acting as the lead programmer, project lead, or project oversight lead for a client/asset. You will play a crucial role in the design, analysis, and reporting of clinical trials, ensuring adherence to regulatory requirements and industry standards.

Key responsibilities include:

  • Serving as a lead programmer or project lead on selected studies or drug programs of all complexity and size scale
  • Maintaining project timelines, assessing and forecasting resources needed, and being accountable for study budgets
  • Representing the company at industry conferences, presenting/teaching at department meetings, and establishing training materials for the department
Requirements

To be successful in this role, you will need:

  • A Master's degree in computer science, statistics, biostatistics, mathematics or a related field, or a Bachelor's degree with equivalent experience and qualifications
  • At least 6 years of clinical trial experience as a statistical programmer and at least 1 year of leadership experience
  • Expert-level knowledge of SAS or more programming languages, SDTMS/ADaMs /TLFs specifications and programming, and Pinnacle 21
  • Strong organizational skills, ability to work in a multi-disciplinary team setting, and excellent written and verbal communication skills
About Us

Thermo Fisher Scientific is an innovative, forward-thinking organization that offers competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. We prioritize integrity, intensity, involvement, and innovation in everything we do.

Estimated salary: $120,000 - $180,000 per annum, depending on location and experience.