Virtusa
Statistical Programmer
Job Description
JD:
Bachelor's or Master's degree in statistics, biostatistics, computer science, or a related field.
Minimum of 7-10 years of experience in statistical programming in the pharmaceutical, biotechnology, or clinical research industry.
Implements statistical programming aspects of the protocol or clinical development program
Proficiency in SAS programming; experience with R, Python, or other programming languages is a plus.
Strong understanding of statistical methods and clinical trial design.
Excellent problem-solving skills and attention to detail.
Effective communication and interpersonal skills, with the ability to collaborate effectively in a cross-functional team environment.
Demonstrated ability to manage multiple priorities and deliver high-quality results within tight timelines.
Experience working in a regulated environment and knowledge of regulatory requirements for clinical research (e.g, FDA ICH EMA is desirable.
Certification in SAS programming or related areas is preferred.
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