Statistical Programmer II, SAS experience

November 14

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Parexel

Regulatory and product development consulting • early phase clinical research • phase II-III clinical research • late phase clinical research • eClinical solutions

10,000+

💰 Venture Round on 1990-01

Description

• Provides technical expertise for clinical trials • Supports programming activities related to clinical data analysis • Assists in project management and documentation • Maintains regulatory compliance and supports audits • Participates in process and quality improvements

Requirements

• Proficient in SAS • Experience in Clinical Research (CRO/Pharma/Biotech/Academia) • Experience in 4GL language • Knowledge of SOPs/Guidelines, ICH-GCP, and other applicable regulations • Attention to detail with a focus on quality • MSc/PhD degree in statistics, econometrics, mathematics, informatics • Excellent analytical skills • Ability to learn new systems • Ability to work as part of a global team • Effective time management skills • Commitment to high-quality work • Customer focus and problem-solving skills

Benefits

• Competitive financial packages • Training and development • Smooth induction and training program • Healthy work/life balance

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