Clinical Database Developer / Programmer

Job DescriptionJob DescriptionWe are seeking a Clinical Database Developer / Programmer to support the transition to a new clinical trial technology platform and help establish a more centralized approach to clinical study builds.Mainly Remote (onsite 1 time per quarter in Philadelphia)Contract to hire$50-55 / HR + Benefits optionsResponsibilitiesReview and interpret clinical trial protocols and study requirements.Build and configure electronic case report forms (eCRFs) used to collect clinical trial data.Translate clinical research requirements into appropriate forms, fields, and study structures.Select and configure standardized forms and fields from existing/global libraries where appropriate.Configure study components within the clinical trial platform using primarily no-code/low-code, drag-and-drop functionality.Build the initial study/protocol and work closely with Wallace and the broader clinical research team to establish an effective study-build process.Ensure forms accurately reflect protocol requirements and required clinical data collection.Perform testing and validation of newly configured forms and study workflows.Participate in user acceptance testing and help identify opportunities for testing automation.Troubleshoot issues related to form configuration, study setup, and data collection.Recommend an approach for efficiently building and maintaining future clinical studies.Communicate regularly through Microsoft Teams, Slack, and other collaboration tools.Support other clinical systems or study-related work as workload permits.Required QualificationsProfessional experience supporting clinical research or clinical trials.Hands-on experience building or configuring clinical studies within an Electronic Data Capture (EDC) or comparable clinical trial platform.Experience designing, building, or maintaining electronic Case Report Forms (eCRFs).Ability to read and understand clinical trial protocols and translate protocol requirements into electronic data-collection forms.Understanding of clinical study workflows and how clinical information is collected throughout a trial.Experience working within a pharmaceutical, biotechnology, CRO, academic research, or comparable clinical research environment.Experience testing and validating clinical forms or study configurations.Strong attention to detail and ability to work independently.Strong communication skills and ability to collaborate directly with clinical research and technology stakeholders.Ability to travel to Philadelphia for an initial onsite meeting and approximately once per quarter thereafter.Preferred QualificationsExperience with Veeva clinical applications,Medidata Rave, or similar tools.Experience with Oracle Clinical or a comparable clinical EDC platform is preferred.Experience working with global libraries, standard forms, reusable fields, or standardized clinical data-collection components.Previous experience supporting study builds within a CRO such as ICON or PPD/Thermo Fisher Scientific.Experience supporting multiple clinical studies or protocols.Experience with UAT and/or automated testing of clinical study configurations.Experience helping establish study-build standards, processes, or best practices. #INDGEN#ZR