Technical Project Manager, Merative US LP, Ann Arbor, MI and various unanticipated client sites throughout the US (Up to 100% telecommuting permitted): Perform project level software configuration validation leveraging the internal clinical data management platform. Work with the Research and Development Team (R&D) and perform custom code testing for software configurations. Build clinical study designs within the software platform. Work with a study design lead, assist with the configuration of clinical software to meet customer requirements within the allotted timelines. Create and implement testing plans for software. Participate in assisting with the execution of test scenarios for studies that were configured by someone else and review studies with completed testing to verify that testing was carried out in accordance with GxP guidelines, which are meant to encompass a collection of quality guidelines in the clinical space. Performs study level configuration testing of clinical trial databases which includes using industry standards and Boolean/programmatic logic to validate the clinical trial database design. Utilize: Software Validation, Software Engineering, Healthcare related software validation, Project Management, Process Improvement methodology, Clinical data management platform (CDM). Required: Bachelor's degree or equivalent in Computer Science, Computer Engineering, Data Science, Software Engineering, Quality Management or related and two (2) years of experience as a Project Manager or related. Two (2) years of experience must include utilizing Software Validation, Software Engineering, Healthcare related software validation, Project Management, Process Improvement methodology, Clinical data management platform (CDM). Please send resumes to AskHR@merative.com. Applicants must reference AV168 in the subject line.