Solutions Design Analyst

Accountabilities: Coordinate the end-to-end Solutions Design Process for clinical studies, ensuring designs meet client expectations and project requirements. Review clinical trial protocols and related documentation to identify study-specific needs and define appropriate eCOA solution designs. Gather and analyze sponsor requirements, recommending the most suitable solution components to address clinical and operational objectives. Develop, maintain, and manage detailed design specifications, ensuring consistency across data capture processes, delivery systems, and database structures. Collaborate with cross-functional teams, including Project Management, Data Management, Product, and Clinical Systems Translation & Licensing, to align requirements and maintain data integrity. Present proposed solution designs during internal and external project milestone meetings, clearly communicating design decisions and recommendations. Support project scoping activities, change control procedures, and testing processes to ensure accurate and efficient implementation. Contribute to continuous improvement initiatives focused on enhancing products, workflows, and solution design processes. Maintain accurate and organized project documentation while supporting study tracking and overall delivery coordination. Requirements: Bachelor's degree (BA/BS) or equivalent combination of education and experience. A degree in science, healthcare, or a related discipline is preferred. At least 3 years of professional experience in clinical trials, clinical research, or a comparable role. Must reside in and work from the Eastern Time Zone (EST/EDT) within the United States. Ability to interpret and analyze clinical trial documentation, including study protocols, questionnaires, and data models. Demonstrated experience translating client or sponsor requirements into clear, structured, and actionable design specifications. Understanding of clinical research standards, FDA regulatory processes, and the requirements governing clinical trial data. Strong communication and interpersonal skills, with the ability to collaborate effectively across multidisciplinary teams and interact confidently with clients and stakeholders at different organizational levels. Excellent organizational and time-management abilities, with the capacity to manage multiple projects and competing priorities in a fast-paced environment. Strong analytical thinking, problem-solving capabilities, and exceptional attention to detail. Ability to work independently, take initiative, and remain adaptable when managing evolving project requirements. Proficiency in Microsoft Office Suite; familiarity with technical documentation tools is an advantage. Benefits: Full-time, remote working opportunity within the Eastern United States. Opportunity to contribute to innovative clinical research and technology solutions that support the development of life-changing therapies. Exposure to pharmaceutical and biotechnology projects and collaboration with multidisciplinary experts in science, technology, and clinical operations. Opportunity to develop expertise in electronic Clinical Outcome Assessments (eCOA), clinical trial processes, and digital clinical solutions. Collaborative and internationally connected professional environment. Opportunity to contribute to continuous improvement and innovative solution design initiatives.