Sr. Solutions Design Analyst, Trial Oversight
San Jose
hace 3 horas

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives.

We value the contribution each of our people brings. It’s only through our people that we can continue to innovate technology that will shape the future of clinical trials.

Clario's Solutions Design Analyst is responsible for delivering the highest quality BI solutions design consultation to our pharmaceutical / biotechnology industry clients.

The Solutions Design Analyst will be aligned with one or more project teams as well as interface with clients, eClinical vendors, and Clario solutions delivery leadership.

The Solutions Design Analyst will ensure that clinical protocols are mapped to BI solutions efficiently, accurately, and within the project scope.

Clario's Sr Solutions Design Analyst will :

  • Coordinate the overall Solutions Design Process ensuring that clinical protocols are appropriately mapped to BI solutions efficiently, accurately, and within the project scope
  • Develop and communicate design best practices for BI solutions
  • Gather and document sponsor and / or eClinical vendor requirements and specify design components to support those requirements
  • Create and maintain specifications for study-specific implementations of BI products and services using a Documentation Management System
  • Ensure consistency between trial data capture, data delivery and database structures to meet client requirements - Responsible for the overall management of the Design Process including communication of design requirements internally and externally with the Customer and eClinical Vendors.
  • This includes participation in internal and external design milestone meetings

  • Track Design related milestones and timelines - Support Solutions Validation / Quality Control testing by addressing any defects associated with the design in a timely manner
  • Collaborate with other departments to investigate study issues found beyond the start-up phase of the study
  • The duties and responsibilities listed in this job description represent the major responsibilities of the position. Clario reserves the right to amend or change these duties.

    Other duties and responsibilities may be assigned, as required. This job description and any attachments do not constitute or represent a contract.

    What we seek :

  • BS, BA, or equivalent (Degree in science / healthcare-related field a plus)
  • Minimum of 3 years of experience in the execution of clinical trials or equivalent
  • Ability to understand and interpret clinical trial documentation such as protocols, clinical data models, and other eClinical data collection instruments
  • Demonstrated experience in interpretation of client requirements to prepare and document design specifications
  • Proven experience in client relations and interactions with clients at all levels
  • Familiarity with FDA regulatory processes, clinical research processes
  • Self-directed - comfortable working in a fast-paced environment
  • Ability to manage multiple project tasks and deliverables
  • Proven problem-solving skills and attention to detail
  • We look forward to receiving your application.

    Interested in working for Clario but this isn't quite the right job for you? Please see our website for our other current openings.

    All are welcome - join us!

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