A leading IT staffing company is seeking an Analysis Standards Associate to manage analysis standards for clinical research. Responsibilities include aligning standards with business needs, reviewing statistical datasets, and supporting stakeholders in implementing these standards. Candidates should hold a BS/BA in statistics and have over 5 years of experience in a biopharma environment, alongside solid SAS programming knowledge. This role also requires strong communication and organizational skills in a collaborative virtual team setting.
Qualifications
5+ years in a statistician role with clinical research analysis.
Basic knowledge of SAS programming for QC/validation.
Understanding of clinical research analysis principles.
Responsibilities
Define and maintain standard statistical requirements.
Review standard datasets and metadata for compliance.
Develop documentation on standards and processes.
Skills
SAS programming
Communication skills
Collaboration
Problem-solving skills
Education
BS/BA degree in statistics or related field
Job description
A leading IT staffing company is seeking an Analysis Standards Associate to manage analysis standards for clinical research. Responsibilities include aligning standards with business needs, reviewing statistical datasets, and supporting stakeholders in implementing these standards. Candidates should hold a BS/BA in statistics and have over 5 years of experience in a biopharma environment, alongside solid SAS programming knowledge. This role also requires strong communication and organizational skills in a collaborative virtual team setting.