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The Project Design Manager I translates complex clinical protocols into system requirements for DDC and eCOA platforms. They lead internal and customer-facing meetings to oversee the study build process and manage User Acceptance Testing (UAT).
Responsibilities
- Review client protocols and other project documentation to assess the scope of the build and communicate it to the appropriate internal teams
- Complete/oversee eCOA builds
- Work with Study Operations Leads to identify needs and resources for study build
- Define system requirements (i.e. application configuration, form content, metadata, and functionality) based on protocol, data collection needs, data export requirements, regulatory guidelines for collecting source data/applicable standards, and application functionality
- Update study requirements throughout the design process as needed
Requirements
- Bachelor’s degree in clinical trial design or equivalent work experience
- Ability to identify needs/issues, track progress, and follow through on actions to meet customer satisfaction
- Excellent written, verbal, and interpersonal communication skills
- Strong organizational skills, attention to detail and ability to multi-task are required
- Experience with MS Office including Word and Excel
Key Skills
About Clinclinicalink
Clinical ink is the global life science company that brings data, technology, and patient-centric research together. Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancements, drive the industry standard for data precision and usher in a new generation of clinical trials. By harnessing digital data, we power sponsors, CROs, researchers, and patients to recenter decentralized trials and rewrite the clinical development experience.
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