Solutions Design Analyst

clarioclinical; United States; Remote; USD 90,000 - 130,000; Full time

Job summary

clarioclinical seeks an experienced professional to design electronic clinical outcome assessment (eCOA) solutions for clinical studies. You will translate trial protocols into study-specific specs and coordinate with project, data, product, and clinical systems teams to ensure accurate implementation and delivery.

The role requires interpreting protocols, documenting requirements, and presenting designs at milestones. Strong communication and regulatory familiarity are essential for success.

Qualifications

• Three years minimum in clinical trials or equivalent role.
• Based in the Eastern Time zone.
• Ability to translate protocols into design specs.
• Strong communication and collaboration with clients at all levels.

Responsibilities

• Coordinate solution design from protocol to design docs.
• Interpret trial protocols and data models to identify requirements.
• Gather sponsor needs and propose suitable components.
• Create and maintain specifications for data capture and databases.
• Coordinate with PM, DM, product, and clinical systems translation teams.
• Present designs and contribute to scoping, testing, and documentation.

Skills

Clinical trial experience

Regulatory knowledge

Communication skills

Documentation skills

Attention to detail

Stakeholder collaboration

Education

Bachelor's degree in science or healthcare

Tools

Office productivity software

Job description

Role overview

Design electronic clinical outcome assessment (eCOA) solutions for clinical studies, translating trial protocols and sponsor needs into clear, study-specific specifications. You will coordinate the design process and work with project, data, product, and clinical systems teams to support accurate implementation and delivery.

Responsibilities

• Coordinate solution design for client studies, from protocol review through design documentation.
• Interpret trial protocols, questionnaires, and data models to identify study requirements.
• Gather sponsor needs and recommend suitable components for each study design.
• Create and maintain specifications that align data capture, delivery, and database structures.
• Coordinate with project management, data management, product, and clinical systems translation teams to align requirements and protect data integrity.
• Present designs at project milestones and contribute to scoping, change control, testing, documentation, study tracking, and process improvement.

Requirements

• Bachelor’s degree or equivalent; a science or healthcare-related degree is preferred.
• At least three years of clinical trial experience or experience in an equivalent role.
• Based in the Eastern Time zone.
• Able to interpret clinical trial documents and translate client requirements into design specifications.
• Strong communication and collaboration skills, including experience working with clients at different levels.
• Familiarity with regulatory processes and clinical research standards; strong organization, problem-solving, and attention to detail.
• Proficiency with office productivity software; experience with technical documentation tools is helpful.