Solutions Design Analyst
Clario
Summary
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.
Job description
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.
Requirements
- 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
- 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
- Excellent problem-solving skills and attention to detail
- Proficiency in MS Office Suite
- Experience with technical documentation tools a plus
Company overview
Clario is a leading provider of technology solutions for clinical trials, offering comprehensive services that support pharmaceutical, biotechnology, and medical device companies throughout the drug development process. The company specializes in electronic clinical outcome assessments (eCOA), cardiac safety solutions, medical imaging services, and endpoint management. With decades of experience in the clinical research industry, Clario combines scientific expertise with advanced technology platforms to deliver reliable data collection and analysis services. Their solutions help streamline clinical trial operations, improve data quality, and accelerate drug development timelines. Clario's global presence and integrated technology ecosystem make it a trusted partner for organizations conducting complex clinical studies across various therapeutic areas, from early-phase research to post-marketing surveillance.