ROLE AND RESPONSIBILITIES Draft, prepare, create, document, and maintain study databases and electronic CRF (eCRF) designs in alignment with protocol and applicable standards. Ensure accurate creation and maintenance of CRFs and questionnaires in consultation with Project Leads. Coordinate and/or lead User Acceptance Testing (UAT) for assigned studies, ensuring thorough documentation and compliance. Communicate with Clients for project-specific operational activities and ensure clear communication with internal teams. Provide oversight and manage relationships with external vendors, ensuring adherence to timelines and quality standards. Establish, maintain, and track data management study timelines in coordination with project teams. Provide technical expertise and justification for direct negotiations with customers on timelines, processes, and resources. QUALIFICATIONS AND EDUCATION REQUIREMENTS 3+ years of experience in clinical data programming, database development, and data management within the Medical Device or CRO industry. Bachelor’s degree in Computer Science, Life Sciences, or a related field. iMedNet database development experience. PREFERRED SKILLS Proficiency in programming and other database management tools. Experience with clinical trial processes and regulatory requirements. Job Type: Full-time Benefits: 401(k) Health insurance Compensation Package: Performance bonus Schedule: 8 hour shift Experience: iMedNet: 2 years (Required) Clinical Database Programming: 3 years (Required) Work Location: Remote