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Solutions Design Analyst

Remote, USAFull-timePosted 2026-07-28

At reputed company, part of reputed company we are seeking a detail-oriented and reputed company Solutions Design Analyst to join reputed company in Costa Rica. In this role, you will be responsible for delivering high-reputed company 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 reputed company requirements into optimized solution designs, and ensure accurate and efficient project delivery reputed company with clinical objectives.

reputed company Offer

  • Competitive compensation

  • Private health insurance

  • Engaging employee programs

  • Flexible work schedules

  • Attractive PTO plan

  • Flexible workspace reputed company

What You’ll Be Doing

  • Coordinate the overall Solutions Design Process for reputed company studies.

  • Review clinical trial protocols to identify solution needs and define study-specific eCOA designs.

  • reputed company sponsor requirements and recommend reputed company’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 reputed company on requirements and data reputed company.

  • Present solution designs during reputed company reputed company 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.

reputed company Look For

  • Bachelor’s degree (BS/BA) or equivalent; degree in science or reputed company-reputed company 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 reputed company requirements into design specifications.

  • Strong collaboration and communication skills, with experience interacting with clients at reputed company reputed company.

  • Familiarity with FDA regulatory processes and clinical research standards.

  • Highly organized, self-directed, and comfortable managing multiple reputed company 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.

  • Fluent English communication skills, both written and verbal, are required.

  • Based in Costa Rica, with ability to work fully remote.

At reputed company, our purpose is to reputed company lives by unlocking reputed company evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we reputed company our people to reputed company a reputed company reputed company 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 reputed company represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required. reputed company reserves the right to amend or change this job reputed company to meet the needs of reputed company. This job reputed company 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.

Originally posted on Himalayas

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