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.