Senior Clinical Trials Programmer and Team Lead

3 days ago

London, Greater London, United Kingdom Lifelancer Full time
Lead a Dynamic Team in Clinical Trial Programming

We are seeking an experienced Clinical Trials Programmer to lead our dynamic team. As a Senior Clinical Trials Programmer and Team Lead, 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. This role plays a crucial part in the design, analysis, and reporting of clinical trials, ensuring adherence to regulatory requirements and industry standards.

About the Job
  • Serves as a lead programmer or project lead on selected studies or drug programs of all complexity and size scale, working directly with teams and clients to conduct team meetings, develop and maintain project timelines, assess and forecast resources needed, and is accountable for study budgets and familiar with any relevant contractual obligations or limits with our clients.
  • May serve in a senior project oversight role on selected projects.
  • May serve in a contributor or reviewer role of key submission materials for regulatory authorities.
  • Provides general infrastructure support to the department, including representing the company at industry conferences, presenting/teaching at department meetings, establishing training materials for the department, contributing to documents or policies, and contributing to process improvement and department initiatives.
Requirements

This position requires a strong understanding of programming technology and techniques, clinical trials, and developments in the pharmaceutical industry. The ideal candidate should have:

  • A Master's degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field, with at least 3 years of experience providing the knowledge, skills, and abilities to perform the job requirements, or a Bachelor's degree in Computer Science, Statistics, Biostatistics, Mathematics, or a related field, or equivalent, with at least 5 years of experience providing the knowledge, skills, and abilities to perform the job requirements.
  • At least 6 years of clinical trial experience as a statistical programmer and at least 1 year of leadership experience, preferably with expertise in Clinical Pharmacology programming.
  • Excellent written and verbal communication skills, including proficiency in English.
  • Strong organizational skills across individual projects, capable of independently and effectively organizing and managing own and team work loads, and completing multiple assignments with challenging timelines.
  • Able to adapt and adjust to changing priorities, contribute to the development of policies, and make decisions regarding programming on company policies and procedures.

The estimated salary for this position is $120,000 - $150,000 per year, depending on location and experience. This role offers remote working flexibility in Europe.

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