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Job summary
A global clinical research firm is seeking a Statistical Programmer II to join their expanding team in Manila, Philippines. This remote opportunity offers candidates a chance to contribute to high-quality data management and statistical programming in clinical trials. Ideal applicants will possess a Master's or Ph.D. in relevant fields and have at least two years of experience in the clinical research domain, including proficiency in SAS programming. Join a committed team impacting clinical research operations worldwide.
Qualifications
At least two years of experience in clinical trial statistical programming and/or data analysis.
Must have knowledge of pharmaceutical clinical research industry standards.
Experience in developing and validating statistical output reports.
Responsibilities
Develop and review SDTM and ADaM dataset specifications.
Program and validate SDTM and ADaM datasets.
Develop and test SAS programs for clinical trial database checks.
Document data and programming information for compliance audits.
Provide technical guidance to less experienced programmers.
Skills
Statistical programming
Data analysis
SAS programming
Clinical trial knowledge
Quality compliance
Education
Master's or Ph.D. in relevant field
Tools
SAS
Job description
A global clinical research firm is seeking a Statistical Programmer II to join their expanding team in Manila, Philippines. This remote opportunity offers candidates a chance to contribute to high-quality data management and statistical programming in clinical trials. Ideal applicants will possess a Master's or Ph.D. in relevant fields and have at least two years of experience in the clinical research domain, including proficiency in SAS programming. Join a committed team impacting clinical research operations worldwide.