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.

Are you ready to make a real difference?

Clario-Costa Rica has a Solutions Design Analyst opportunity ! In this role, you will take responsibility for delivering the highest quality eCOA solutions design consultation to our pharmaceutical / biotechnology industry clients.

You will align with our project teams and interface with clients and Clario solutions delivery leadership to ensure that clinical protocols are mapped to software solutions efficiently, accurately, and within project scope.

As a Solutions Design Analyst, your essential work will include :

Coordinating the overall Solutions Design Process for our clients (Trial Sponsors)

Gathering sponsor requirements and suggesting Clario's best design components to support those requirements

Creating and maintaining specs for study-specific implementations

Ensuring consistency between trial data capture, data delivery and database structures to meet client requirements

Managing the Design Process including communication of design requirements internally and externally with the Customer. This includes participation in internal and external design milestone meetings

Collaborating with internal teams such as Project Management (to establish and refine scope definitions), Clinical Systems Translation & Licensing (CSTL) (on proper trial questionnaires) and Data Management to ensure the right data is collected to satisfy the sponsor's study needs

Collaborating with other departments for testing requirements; to support related study issues, and to assist with project scoping and / or change control processes

Supporting Product Development, Process Development and Study tracking efforts

The duties and responsibilities listed in this job description represent the major responsibilities of the position. Other duties and responsibilities may be assigned, as required.

Clario reserves the right to amend or change this job description to meet the needs of Clario. 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, questionnaires and other data collection instruments, and clinical data models

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

Excellent presentation, communication (written and oral) and negotiation skills

Ability to travel up to 25%

Local to Costa Rica

Ability to work from home on a regular basis (this role will be fully remote to start, although we may offer hybrid options at a later date)

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.

LI-DNI