Solutions Design Analyst

hace 4 semanas

San José, Costa Rica Clario A tiempo completo

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

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