Solutions Design Analyst, Specialty Solutions

Job description

At Clario, part of Thermo Fisher Scientific. Join us in making clinical trials easier, faster, more engaging, and accessible to all. We are transforming the future of clinical trials. Our Specialty Solutions & Clinical Adjudication team supports some of the world’s most complex and meaningful studies, helping sponsors bring life‑changing therapies to patients faster. We’re looking for passionate Solutions Design Analysts to join our growing team in India. If you have an academic background in Life Sciences and hands-on experience with eCOA, ePRO, IRT/RTSM, eConsent, or other clinical technologies—and you’re excited about designing systems that directly improve patient and investigator experience—this is the role for you. What We Offer Competitive compensation + shift allowances Comprehensive benefits supporting security, flexibility, wellbeing, and work–life balance Engaging employee programs and learning opportunities Hybrid working technology and excellent onsite facilities What You’ll Be Doing As a Solutions Design Analyst, you will be a key part of our project teams and will take responsibility for delivering the highest quality solutions design consultation to our clients across the world. In this role you will: Manage & Coordinate the overall Solutions Design process ensuring that clinical protocols are appropriately mapped to software solutions efficiently, accurately and within project scope Gather and document requirements and specify design components to support those requirements; Representing the Solutions Design team and provide subject matter expertise within client facing meetings as required Create and maintain specifications for study-specific implementations of Clario products and services Ensure consistency between trial data capture, data delivery and database structures Collaborate with Clinical Systems Translation & Licensing to confirm correct versions of copyrighted questionnaires are implemented Support Solutions Validation/Quality Control testing by addressing any defects associated with the design in a timely manner Collaborate with other departments to investigate study issues found beyond the startup phase of the study Provide input to interdepartmental process improvement initiatives Collaborate with Clinical PM to ensure sponsor needs are met from system perspective Participate or lead parts of internal and external design milestone meetings Serve as additional delegate representing Solution Design in client audits to describe process flows, standards and best practices Partner with other Clario teams - such as business Development and Project Management – to assist in reviewing & analyzing proposals & protocols for new studies Configure systems to map to configurational documents What We Look For BSc, MSc, PhD in a subject related to the Pharmaceutical / Healthcare / Life Science industry or Computer Sciences A demonstrable understanding of eClinical systems and Clinical Research Experience working in an international environment and managing client relations at all levels Strong verbal & written communication skills (English Language) Experience working in Clinical Research as a Clinical Research Associate (CRA) / Clinical Research Manager Business Analyst or Project Coordinator / Project Manager (or similar positions) is highly desirable Previous experience working with with Clinical Adjudication, eCOA / ePRO, IRT/RTSM, eConsent, or other eClinical / Clinical / Healthcare technology solutions is highly desirable A genuine interest in and passion for Software Design and and patient focused research At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.