En Humand, ayudamos a las empresas a digitalizar sus procesos de comunicación interna, cultura y recursos humanos en un solo lugar.
¿Te gustaría ser parte de la revolución digital en tecnología?
Estamos buscando un/a React Engineer con muchas ganas de sumarse al equipo y aportar en la creación de productos innovadores y escalables.
En este rol, serás responsable de desarrollar interfaces de usuario efectivas que maximicen la experiencia de nuestros usuarios y colaboran con nuestro crecimiento.
Principales Responsabilidades
Desarrollar y optimizar componentes y aplicaciones frontend usando React y TypeScript.
Colaborar con los equipos de diseño y producto para ofrecer una experiencia de usuario intuitiva y de alto rendimiento.
Asegurar que las aplicaciones sean rápidas, accesibles y escalables, manteniendo buenas prácticas de desarrollo.
Participar en la definición y planificación de nuevas funcionalidades, alineadas con nuestros objetivos de calidad y usabilidad.
¿Qué valoramos?
Experiencia en desarrollo frontend con React y TypeScript.
Conocimiento en arquitectura de componentes y diseño de interfaces.
Habilidad para trabajar de manera colaborativa con equipos multidisciplinariosical training sessions according to the project specific requirements.
May prepare or assist in preparation of study-specific presentations/training materials and tools
Assists the team managers in the preparation and review of protocols and other study documentation
Supports the design and development of CRFs and clinical trial documents as they pertain to clinical monitoring activities (i.e. operating manuals, monitoring guidelines, etc.)
Assists with review of clinical study reports
Functions as a mentor,



assisting with the training and developing of new employees and junior monitors
Interacts with client, participates in proposal activities, including development and client presentations
Initiates payment requests for investigators
Travels as necessary according to project needs
Other job duties as assigned
4-year college degree or equivalent experience in a scientific or healthcare discipline
5 years or more as a CRA in either a CRO or pharmaceutical/ biotech industry or equivalent, relevant experience and/or demonstrated competencies
Significant site management experience or equivalent experience in clinical research
Ability to communicate both verbally and in writing at the English proficiently (Professional level)
Preferred Education & Experience:
Experience monitoring in rare and complex therapeutic areas
Experience monitoring EDC trials and EHR records
Experience in biopharma or relevant therapeutic area
Relevant site start-up (feasibility, contract negotiations, submissions) experience for the country
Ability to monitor study sites, with supervision, according to protocol monitoring guidelines, SOPs, GCP and ICH guidelines
Ability to resolves project related problems and prioritize workload to meet deadlines with oversight from management.
Can assist junior CRAs in problem resolution
Ability to travel overnight.
Up to 60% travel on average, based on regional requirements.




International travel as needed
Select opportunities require Oncology experience preferably in early phases
Exhibits self-motivation and is able to work and plan independently as well as in a team environment.
Understands clinical trials methodology, including a working knowledge of protocols and indications being studied.
Demonstrated ability to conduct formal presentations to a wide variety of audiences including colleagues, investigative staff, and clients with a high level of proficiency.
Demonstrated focus on continuous improvement, including the ability to make proactive assessments on how to make processes more efficient and people more effective.
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📌 Senior React Software Engineer (Neuquén)
🏢 Precision Medicine Group
📍 Neuquén