Lead programmer for one or more clinical validation studies supporting in vitro diagnostic submissions (e.g., IVDR, 510(k), CTA/CDx/PMA, etc.) including dataset and TFL generation; Perform programming validation and maintain documentation as needed; Lead development of programming infrastructure, including R package development and; Contribute to development of junior team members
Requirements:
Bachelor’s in statistics, mathematics, computer science, or related field; 5+ years related experience with at least 3 years experience in Clinical Trial analysis; At least 3 years R programming experience, including package development
Text:
Lead Statistical Programmer Lead programmer for one or more clinical validation studies supporting in vitro diagnostic submissions (e.g., IVDR, 510(k), CTA/CDx/PMA, etc.) including dataset and TFL generation; Perform programming validation and maintain documentation as needed; Lead development of programming infrastructure, including R package development and; Contribute to development of junior team members Bachelor’s in statistics, mathematics, computer science, or related field; 5+ years related experience with at least 3 years experience in Clinical Trial analysis; At least 3 years R programming experience, including package development
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