Solutions Design Analyst

Clario; United States; Hybrid; USD 90,000 - 120,000; Full time

Benefits offered by this job

Competitive compensation

Medical, dental, and vision insurance

Flexible work schedules

Attractive PTO package

Remote and hybrid work options

Job summary

Clario, part of Thermo Fisher Scientific, seeks a detail-oriented Solutions Design Analyst to deliver high-quality eCOA design solutions for pharmaceutical and biotech clients. You will translate client requirements into optimized solution designs, review protocols, and ensure efficient project delivery aligned with clinical objectives.

Responsibilities include coordinating the design process, creating specifications, and collaborating with PM, Data Management, Product, and CSTL teams.

Qualifications

• Bachelor's degree in science or healthcare field.
• Minimum 3 years of clinical trials experience.
• Ability to translate client requirements into design specifications.
• Strong collaboration and communication skills.
• Familiarity with FDA regulatory processes.
• Highly organized, detail-oriented, and able to manage multiple projects.

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 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

Clinical trial design understanding

Client requirements translation

Collaboration and communication

FDA regulatory familiarity

Project management

MS Office proficiency

Education

Bachelor's degree in science/healthcare

Minimum 3 years of clinical trials experience

Tools

MS Office

Design documentation tools

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 We Offer

• Competitive compensation

• Medical, dental, and vision insurance beginning Day 1

• Flexible work schedules

• Attractive PTO package

• Remote and hybrid work options

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.

• 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.