Solutions Design Analyst

Clario is a 50+ year-old industry leader in delivering clinical trial endpoint technology solutions. The future of clinical trials is evolving, and our innovative technologies are revolutionizing efficiency, accuracy, and integration of trial data. From new trial methodologies to faster, more integrated evidence collection, our solutions help unlock better clinical outcomes.

What We Offer

• Competitive compensation

• Private health insurance

• Flexible work schedules

• Attractive PTO plan

• Engaging employee programs

• Flex workspace

What You’ll Be Doing

• Coordinate the overall Solutions Design Process, ensuring clinical protocols are effectively mapped to software solutions.

• Gather and document client requirements, specifying design components to support study needs.

• Create and maintain study-specific specifications using a Documentation Management System.

• Ensure data capture, data delivery, and database structures meet client requirements.

• Lead internal and external design milestone meetings with stakeholders.

• Collaborate with Clinical Systems Translation & Licensing (CSTL) to ensure correct versions of copyrighted questionnaires are implemented.

• Support Solutions Validation/Quality Control (QC) testing, addressing any defects related to the study design.

• Work closely with Data Management (DM) teams to align software solutions with data extraction needs.

• Assist in project scoping, revision management, and change control processes.

• Provide feedback on product functionality to the Product Development team.

• Support audit preparation by researching project-specific information and responding to audit findings.

• Track time for billable and non-billable tasks and maintain project milestones using Clario’s scheduling tools.

• Participate in process improvement initiatives to enhance workflow efficiency.

What We Look For

• Bachelor’s degree (BS/BA) or equivalent experience (Science/Healthcare-related field preferred).

• 5+ years of relevant experience in clinical trials, software solutions, or related fields.

• 3+ years of experience in a clinical indication-specific role.

• 1+ year of experience with sponsor-specific standards.

• Ability to interpret clinical trial documentation (protocols, questionnaires, data models).

• Experience in client relations and engagement with stakeholders at all levels.

• Familiarity with FDA regulatory processes and clinical research methodologies.

• Strong problem-solving skills, attention to detail, and project management abilities.

• Excellent communication, presentation, and negotiation skills.

• Ability to manage multiple tasks in a fast-paced environment.

• Ability to travel up to 25% as required.

EEO Statement

Clario is an equal opportunity employer. We evaluate all qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.