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Solutions Design Analyst

Clario
A tiempo completo
Remoto
Costa Rica

We are seeking a detail-oriented and collaborative Solutions Design Analyst to join our team in Costa Rica. 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 – Costa Rica

  • Competitive compensation

  • Private health insurance

  • Engaging employee programs

  • Flexible work schedules

  • Attractive PTO plan

  • Flexible workspace options (remote/hybrid)

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.

  • Ability to travel up to 25%.

  • Based in Costa Rica, with ability to work fully remote (hybrid options may be available later).

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.

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