Statistical Programmer II

November 8

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Parexel

Regulatory and product development consulting β€’ early phase clinical research β€’ phase II-III clinical research β€’ late phase clinical research β€’ eClinical solutions

10,000+

πŸ’° Venture Round on 1990-01

Description

β€’ Provide technical expertise for clinical trials β€’ Support programming activities for clinical study data analysis and reporting β€’ Ensure compliance with SOPs/Guidelines and participate in audits

Requirements

β€’ Minimum 3 years experience in Clinical Research β€’ Sound SAS programming skills β€’ Knowledge of CDISC standards (SDTM, ADaM)

Benefits

β€’ Competitive financial packages β€’ Training and development β€’ Healthy work/life balance

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