When our values align, there's no limit to what we can achieve.The role can be flexibly based in select European locations.Picture Yourself At Parexel:The role leads the implementation of technology at a clinical trial's outset, ensuring timely start-up, quality delivery, and compliance with the study protocol and client contracted services. The individual has responsibility for oversight and delivery of User Acceptance Testing of clinical systems and associated documentation.What You'll Do At Parexel:Lead the UAT Testing of the eClinical platform for a study.Serve as the primary point of contact internally and with external customers as needed for UAT delivery.Collaborate with Project Leaders, Project Specialists, and other study team members on UAT Testing needs from the point of early trial planning through trial execution if needs change (e.g., under a protocol amendment).Analyze protocols and collaborate with all stakeholders to create and review user requirements and integration needs from the perspective of UAT testing.Identify and mitigate any risks related to system set-up and integrations with internal systems and/or sponsor systems and implement appropriate testing scenarios to mitigate risks.Focus on timely, high-quality delivery of all services provided.Stay current on the latest Parexel technology offerings, integration issues, and relevant clinical trial process developments in the industry.Interact with external clients as needed for discussion on technology set-up, UAT testing, modifications, and integrations.Demonstrate a proactive approach to providing solutions in a timely manner.Maintain a positive, results-oriented work environment, modeling teamwork, and communicating with team members in an open, balanced, and objective manner.Maintain a working knowledge of applicable ICH Guidelines and Good Clinical Practices.Complete routine administrative tasks in a timely manner (e.g., timesheets, training) and in compliance with relevant guidelines.Ideal candidate will possess:Several years of life science industry experience (CRO/Pharma).Experience in leading eClinical software testing.Experience in IRT/RTSM and/or Digital Health Technology system delivery.Ability to manage independently competing priorities with attention to detail.Ability to learn new systems and function in an evolving technical environment.Global virtual team coordination experience for trial technology set-up.Excellent verbal and written communication skills.Ability to work to timelines.Fluent English.Strong customer focus.Knowledge of SOPs/Guidelines/System Life Cycle methodologies, ICH-GCP, and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application.
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