Solutions Design Analyst

Clario; Tate Township (OH); Hybrid; USD 85,000 - 110,000; Full time

Job summary

Clario in the Eastern United States seeks a Solutions Design Analyst to deliver high-quality eCOA solution designs for pharmaceutical and biotechnology clients. You will translate client requirements into optimized designs, review study protocols, and collaborate with cross-functional teams to ensure data integrity and efficient project delivery aligned with clinical objectives.

The role requires a BS/BA in a science or healthcare field, 3+ years in clinical trials, and ET-zone availability.

Qualifications

• Bachelor’s degree in science or healthcare field (or equivalent).
• 3+ years of experience in clinical trials or equivalent role.
• Based in the Eastern Time (ET) zone (EST/EDT).
• Ability to interpret protocols, questionnaires, and data models.
• Translate client requirements into design specifications for eCOA solutions.
• Strong collaboration and communication skills with clients at all levels.
• Familiarity with FDA regulatory processes and clinical research standards.
• Highly organized, self-directed, and capable of managing multiple projects.

Responsibilities

• Coordinate the Solutions Design Process for client studies.
• Review clinical trial protocols to identify design needs and define eCOA designs.
• Gather sponsor requirements and translate into design components.
• Create and maintain design specifications for data capture and databases.
• Collaborate with PM, Data Management, Product, and CSTL to align on requirements.
• Present designs during internal and external milestone meetings.
• Support project scoping, change control, and testing processes.
• Contribute to product and process improvement initiatives.

Skills

Clinical trial experience

Requirements translation

Collaboration & communication

Attention to detail

Project management

ET time zone familiarity

Education

Bachelor's degree in science/healthcare

Tools

MS Office

Technical documentation tools

Job description

Solutions Design AnalystI agree to the Clario **Terms of Use** and **Privacy Policy**.### Solutions Design AnalystApply: Eastern United States Remote: Full time: Posted Yesterday: R18431At 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. **What You’ll Be Doing*** 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. **What We Look For*** 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.* Must be based in the Eastern Time (ET) zone (EST/EDT).* 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. 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. *The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. Clario reserves the right to amend or change this job description to meet the needs of Clario. This job description and any attachments do not constitute or represent a contract.**The Department Head has the discretion to hire personnel with a combination of experience and education, which may vary from the above listed qualifications.*