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Solutions Design Analyst

Remote:

Full Remote

Contract:

Full time

Experience:

Mid-level (2-5 years)

Work from:

Costa Rica

Offer summary

Qualifications:

BS, BA or equivalent degree, Minimum of 3 years in clinical trials, Ability to interpret clinical trial documentation, Experience in client relations, Familiarity with FDA regulatory processes.

Key responsabilities:

Coordinate the Solutions Design Process.
Develop and communicate design best practices.
Gather and document client requirements.
Manage the Design Process and communicate needs.
Track milestones and support quality control testing.

Clario Biotech: Biology + Technology XLarge https://clario.com/

5001 - 10000 Employees

See more Clario offers

Job description

As the Solution Design Analyst you will be responsible for delivering the highest quality BI solutions design consultation to our pharmaceutical/biotechnology industry clients. You will be aligned with one or more project teams as well as interfaces with clients, eClinical vendors and Clario solutions delivery leadership. You will ensures that clinical protocols are mapped to BI solutions efficiently, accurately, and within project scope.

What You'll Do

Coordinate the overall Solutions Design Process ensuring that clinical protocols are appropriately mapped to BI solutions efficiently, accurately and within 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
Collaborates with DM, Solution Design Analysts and eClinical vendors to ensure that the software solution captures the necessary data points for data extraction, visualization and real-time integration
Assist in project scoping and change control processes including revision management
Provide feedback to Product Development group on new product functionality
Provide input to interdepartmental process improvement initiatives
Track time for billable study related and non-billable tasks in a timely manner
Track SDA milestone start and completion dates using the Clario project scheduling tool
Complete activities in the Training Management System in a timely manner

What You Bring

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