Senior Clinical Data Management Specialist

4 days ago

jaipur, India beBeeClinical Full time

Expert Veeva EDC Programmer Job DescriptionThe role involves working with technology vendors to ensure established milestones are met with the highest degree of quality, tracking study deliverables, evaluating study metrics to mitigate risk, and being adaptable to new ways of working using technology to accelerate clinical trial setup.Create electronic case report form (eCRF) specifications, design, develop and validate clinical trial setup process using expertise in Veeva Electronic Data Capture (EDC).Implement edit check specifications, set up edit checks at trial level, and test the setup of the clinical study through user acceptance testing (UAT) scripts.Set up different instances of study URLs (e.g. UAT, production, testing etc.) and configure user accounts for study teams.Manage blinded and unblinded study configurations and be the subject matter expert (SME) for all EDC database related activities.Set up, configure, validate, and integrate other modules within the EDC ecosystem such as coding, integration of interactive response technology (IRT), safety system, local labs etc.Collaborate with Clinical Operations, Clinical Supplies, IT, and Quality organizations to oversee system delivery life cycle.Partner with leaders to resolve issues affecting the delivery of clinical trials and work closely with data engineers and data management programmers on study level integrations and deliveries.Requirements:Expertise in Veeva EDCExperience in clinical trial setup processKnowledge of eCRF specificationsAbility to collaborate with cross-functional teamsStrong problem-solving skillsBenefits:This role offers a unique opportunity to work with cutting-edge technology and contribute to the acceleration of clinical trial setup. As an Expert Veeva EDC Programmer, you will have the chance to work with a talented team and develop your skills in a dynamic and fast-paced environment.

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