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# Solutions Design Analyst

- **Company:** BioClinica
- **Location:** United States (Remote available)
- **Experience:** Experienced
- **Contract:** Permanent contract
- **Skills:** Data Integrity, Database Storage Structures, Microsoft Office, Data Management
- **Published:** August 14, 2026
- **Apply:** https://clarioclinical.wd1.myworkdayjobs.com/clarioclinical_careers/job/United-States-Remote/Solutions-Design-Analyst_R17946

## About the Role

* Bachelor's degree (BS/BA) or equivalent; degree in science or healthcare-related field preferred.
 * Minimum 3 years of experience in clinical trials or equivalent role.
 * Ability to interpret clinical trial documentation such as protocols, questionnaires, and data models.
 * Proven experience in translating client requirements into design specifications.
 * Strong collaboration and communication skills, with experience interacting with clients at all levels.
 * Familiarity with FDA regulatory processes and clinical research standards.
 * Highly organized, self-directed, and comfortable managing multiple projects in a fast-paced environment.
 * Excellent problem-solving skills and attention to detail.
 * Proficiency in MS Office Suite; experience with technical documentation tools a plus.

## Description

At Clario, part of Thermo Fisher Scientific we are seeking a detail-oriented and collaborative Solutions Design Analyst to join our team. In this role, you will be responsible for delivering high-quality eCOA (electronic Clinical Outcome Assessment) solution designs for our pharmaceutical and biotechnology clients. You will work closely with cross-functional teams to review study protocols, translate client requirements into optimized solution designs, and ensure accurate and efficient project delivery aligned with clinical objectives., * Coordinate the overall Solutions Design Process for client studies.

 * Review clinical trial protocols to identify solution needs and define study-specific eCOA designs.
 * Gather sponsor requirements and recommend Clario's best design components to meet study needs.
 * Create and maintain design specifications ensuring consistency across data capture, delivery, and database structures.
 * Collaborate with Project Management, Data Management, Product, and Clinical Systems Translation & Licensing (CSTL) to align on requirements and data integrity.
 * Present solution designs during internal and external milestone meetings.
 * Support project scoping, change control, and testing processes as needed.
 * Contribute to product and process improvement initiatives.
 * Maintain organized documentation and support study tracking efforts.


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