About The Position

Clario, part of Thermo Fisher Scientific, is seeking a detail-oriented and collaborative Solutions Design Analyst to deliver high-quality electronic Clinical Outcome Assessment (eCOA) solution designs for pharmaceutical and biotechnology clients. The role works with cross-functional teams to review study protocols, translate client requirements into optimized solution designs, and support accurate, efficient project delivery aligned with clinical objectives. The analyst coordinates the solutions design process for client studies, identifies study-specific eCOA needs, recommends suitable design components, and creates and maintains design specifications. The role collaborates with Project Management, Data Management, Product, and Clinical Systems Translation & Licensing (CSTL) to align requirements and support data integrity. It also includes presenting designs at milestone meetings, supporting scoping, change control and testing, contributing to product and process improvements, and maintaining documentation and study tracking. The position requires at least three years of experience in clinical trials or an equivalent role and a bachelor’s degree or equivalent. The successful candidate must be based in the Eastern Time zone (EST/EDT).

Requirements

  • Bachelor’s degree (BS/BA) or equivalent.
  • At least 3 years of experience in clinical trials or an equivalent role.
  • Must be based in the Eastern Time (ET) zone (EST/EDT).
  • Ability to interpret clinical trial documentation, including protocols, questionnaires, and data models.
  • Experience translating client requirements into design specifications.
  • Strong collaboration and communication skills, including experience interacting with clients at all levels.
  • Familiarity with FDA regulatory processes and clinical research standards.
  • Highly organized and self-directed, with the ability to manage multiple projects in a fast-paced environment.
  • Excellent problem-solving skills and attention to detail.
  • Proficiency in MS Office Suite.

Nice To Haves

  • A degree in a science or healthcare-related field.
  • Experience with technical documentation tools.

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 Clario design components to meet study needs.
  • Create and maintain design specifications for consistency across data capture, delivery, and database structures.
  • Collaborate with Project Management, Data Management, Product, and Clinical Systems Translation & Licensing (CSTL) to align requirements and support 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.
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