Job Description
Job Description
We 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 options
Responsibilities
- Review 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 Qualifications
- Professional 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 Qualifications
- Experience 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.
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