Principal Statistical Programmer

Contact name: Emily Munn

Contact email: emily.munn@medella.life
Job ref: 562
Published: about 1 year ago
We are pleased to inform you that we have an exciting opportunity for a Principal Statistical Programmer at a small CRO specialising in the management and analysis of clinical data. We are looking for a highly skilled and experienced individual who can lead our statistical programming team and play a key role in the development of innovative clinical trial solutions.

As a Principal Statistical Programmer, you will be responsible for leading the programming activities for complex clinical trials, providing guidance and mentorship to junior programmers, and collaborating with cross-functional teams to ensure that projects are completed on time and within budget.

We are looking for someone with the following qualifications:
 
  • A minimum of 5 years of experience in statistical programming for clinical trials
  • Strong programming skills in SAS, R, and/or Python
  • Experience with CDISC standards and FDA regulations
  • Excellent communication and leadership skills

My client offers a competitive salary and benefits package, as well as opportunities for career development and growth. If you are interested in this opportunity and believe you have the qualifications we are looking for, please submit your resume.