Location: BaselContract duration: 1 yearResponsibilitiesOperate as the core representative for Clinical Data Management on the study team and to be accountable for collectionReview and management of data and ensure deliverables are metLeads the CDM study team and maintains oversight of all build, conduct and close activities for one or more studies, ensuring fit for purpose quality.Implements study conventions, processes, knowledge sharing and best practices on assigned study(s)Actively contribute to EDC system programming and maintenance. BA/BS degree or equivalent and moderate industry-related experience.Practical and theoretical expertise within his or her sub function.Programming and system development expertise required. In-depth understanding of the business of his or her sub function and the wider CDM organization.RequirementsA BA/BS degree (or equivalent) coupled with industry experience (3-5 years) in a clinical research environment.In-depth understanding of CDM business processes and how they align with global regulatory requirements (GCDMP, ICH-GCP, etc.).Expertise in ensuring data is "analysis-ready," requiring a theoretical and practical grasp of data flow from collection to submission.Proficiency in programming (e.g., SQL, SAS, or Python) to collaborate effectively with IT and drive system enhancements.Experience acting as the Primary Point of Contact (POC) & Leadership for CDM in cross-functional settings.
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