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.
What We Do
-- Clario has been named a Top Workplace by Energage for the 2022 Top Workplaces USA national awards. -- Clario generates the richest clinical evidence by fusing our deep scientific expertise and global scale into the broadest endpoint technology platform. By doing this, we empower our partners to transform lives. With almost 50 years of experience, 19,000 clinical trials, and 870 regulatory approvals, Clario has mastered the ability to generate rich evidence across a Trial Anywhere™ portfolio: decentralized (DCT), hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe, and Asia Pacific, Clario delivers the power of certainty. Partners ————— Clario brings the best of ERT and Bioclinica together to work alongside our partners to solve some of their biggest questions on topics such as: - eCOA vs. paper - Decentralized Clinical Trial (DCT) - Rescue a clinical trial - Broad endpoint technology: cardiac safety, imaging, respiratory And many more. People ———— We are so honoured to be named a 2022 Top Workplace by Energage. One of our leading values at Clario is People First Always. We help individuals build meaningful careers at Clario as they serve to help transform patients lives. Join us on this journey and check out our careers page: https://clario.com/careers/
