Solutions Design Analyst

eResearch Technology Inc; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

Clario is seeking a Solutions Design Analyst to deliver high-quality eCOA solution designs for pharmaceutical and biotechnology clients. You will translate client requirements into optimized designs and ensure accurate project delivery aligned with clinical objectives.

Responsibilities include coordinating design processes, reviewing protocols, gathering sponsor requirements, and presenting designs at milestones.

Qualifications

• Bachelor's 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 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 capable of managing multiple projects in a fast-paced environment.
• Proficiency in MS Office Suite; experience with technical documentation tools is a plus.

Responsibilities

• 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 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.

Skills

Collaboration & communication

Translating requirements into design

Attention to detail

Problem-solving

Education

Bachelor's degree in science/healthcare

Tools

MS Office Suite

Job 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.

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.

Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.