VaxTrials, a great

place to work!

We are a company that prioritizes personal relationships, and which is fully committed to providing a great working experience. We are always aiming to create a positive working environment for the personal and professional wellbeing of those who are part of the VaxTrials team.

For those seeking challenges and wishing to contribute to projects in the area of clinical research, VaxTrials offers a welcoming company culture, where professionalism, commitment and effort are recognized. We also offer:

  • Flexibility in the work place

  • Equitable wages for women and men throughout the organization 

  • Growth opportunities in your professional career

  • Keep our top talented people engaged 

  • Employee platforms for resource management, financial and trainings


We are looking for professionals who want to be part of a dynamic company, with a friendly and welcoming workplace culture: professionals with an innovative mindset, the flexibility to easily adapt to changes, who are dynamic, purposeful, passionate, and committed to our mission. We want leaders, individuals of integrity, who are willing to deliver excellent, high-quality results.

Supervise, verify, inform, and control the activities at each of the investigation sites, to guarantee that the objectives of each clinical study are fulfilled.

Prerequisites :
Education level: Professional
Specific field: Health or related areas
Experience: 1 to 5 years of clinical investigation monitoring. (Depending on seniority; Junior – Senior)

Regulating the clinical investigation according to the country where the study is supervised. Knowledge of the clinical investigation environment, GCP, English, and Microsoft Office tools. (Excel, Word, PP), Technological Solutions (CRF, DIARIES)

For further information, please contact us at

Apply Now!
Support and execute the Clinical Operations Manager’s activities. Define, direct, evaluate and follow up on clinical investigation projects’ development to ensure their execution and that they fulfill all the legal and internal/external quality control requirements.

Education level: University degree
Specific field: Health or related areas
Experience: 2 years of experience in clinical investigation

Clinical investigation, GCP, Database management, Clinical monitoring, Regulatory standards (FDA, LOCAL REGULATION), Budget management and negotiating with providers and The Investigation Centre, Internal solutions (PFS, Trial Pal etc.) English, Google Drive – Office tools (Excel, Word, PP).

For further information, please contact us at

Our company is growing and looking for the best talent!

We need a CRA Manager who is responsible for:

  • The selection, incorporation, training, evaluation, daily line management, development and provision of resources of the team in charge

  • Must hire / evaluate (new) team members (CRA, CTA), ensuring they are adequately qualified for their role and tasks and suggest and develop improvements to systems and processes

  • More than 10 years of previous experience in the clinical operations industry, including more than 5 years of monitoring. High level of understanding of clinical research and clinical trial management and associated local regulatory processes and quality requirements

  • More than 1 year of experience as a line manager or supervisor

  • Great knowledge and ability to apply the applicable clinical research regulatory requirements; that is, Good Clinical Practice guidelines (GCP) and International Conference on Harmonization (ICH)

  • The candidate must speak Spanish / English and the person's location can be in any country in Latin America 

For further information, please contact us at

¡Nuestra compañía se encuentra en crecimiento y busca los mejores talentos!

Necesitamos un CRA Manager que sea responsable de:

  • La selección, incorporación, capacitación, evaluación, gestión de línea diaria, desarrollo y dotación de recursos del equipo a cargo

  • Debe contratar / evaluar (nuevos) miembros del equipo (CRA, CTA), asegurándose de que estén adecuadamente calificados para su función de tareas, sugerir, desarrollar mejoras a sistemas y procesos

  • Más de 10 años de experiencia previa en la industria de operaciones clínicas, incluidos más de 5 años de monitoreo. Alto nivel de comprensión de la investigación clínica y la gestión de ensayos clínicos y los procesos regulatorios locales asociados y los requisitos de calidad

  • Más de 1 año de experiencia como gerente de línea o supervisor

  • Gran conocimiento y habilidad para aplicar los requisitos reglamentarios de investigación clínica aplicables; es decir, directrices de Buenas Prácticas Clínicas (GCP) y International Conference on Harmonization (ICH)

  • El candidato debe hablar español/inglés y la localización de la persona puede ser en cualquier país de Latinoamérica

 Para obtener más información, comuníquese con nosotros en

We want you to be part of our team!

Our company wants to find the best Project Manager with experience in clinical trial research:

  • +10 years of previous experience in clinical / industry operations, including more than 2 years of monitoring, High level of understanding of clinical research, in the management of clinical trials, quality, processes and associated local regulations

  • +5 years of experience as a project manager or supervisor, directly or indirectly managing a project team

  • Project / Process Management Certificate (PMP / Six Sigma) (preferably)

  • Management of phase 3 studies with or in CRO

  • You are skillful, you learn quickly, you are proactive, it is your strength to boost performance in the work team

  • Your level of Excel skills is advanced; you do BI reports and your English level is intermediate-advanced

  • You are in any country in Latin America.

For further information, please contact us at

¡Queremos que hagas parte de nuestro equipo!

Nuestra compañía quiere encontrar al mejor Project Manager con experiencia en investigación de estudios clínicos:

  • +10 años de experiencia previa en operaciones clínicas / industria, incluidos más de 2 años de monitoreo

  • Alto nivel de comprensión de la investigación clínica, en la gestión de ensayos clínicos, calidad, procesos y normativos locales asociados

  • +5 años de experiencia como gerente o supervisor de proyectos, administrando directa o indirectamente un equipo de proyecto

  • Certificado de Gestión de Proyectos / Procesos (PMP / Six Sigma) (preferiblemente)

  • Gestión de estudios de fase 3 con o en CRO

  • Eres hábil, aprendes con rapidez, eres proactivo, es tu fuerte impulsar el rendimiento en el equipo de trabajo

  • Tu nivel para el manejo de Excel es avanzado, realizas informes de BI y tu nivel de inglés es intermedio-avanzado

  • Estas ubicado en cualquier país de Latinoamérica 

 Para obtener más información, comuníquese con nosotros en

¡We are in search of the Best!

For our team, we are looking for a professional with extensive experience in imports with studies in clinical research, preferably in vaccines; knowledge in regional regulation of the countries of Latin America and Central America in imports and exports, maintenance of Import Licenses, handling and triangulation at the logistics level of various suppliers.  Logistics and the inventory of the research product and clinical study supplies, knowledge of the re-labeling process.

For further information, please contact us at

¡Estamos en búsqueda del mejor!

Para nuestro equipo estamos buscando un profesional con amplia experiencia en importaciones con estudios en investigación clínica, preferiblemente en vacunas; conocimiento en regulación regional de los países de Latinoamérica y Centro América en importaciones y exportaciones, mantenimiento de Licencias de Importación, manejo y triangulación a nivel logístico de varios proveedores.

Logística e inventario de producto en investigación y suministros de estudios clínicos, conocimiento del proceso de re-etiquetado.

Posición remota. Nivel de inglés Avanzado. 

Para obtener más información, comuníquese con nosotros en

We are looking for you!

If you are a professional graduated in administrative or financial areas, you have 2 to 3 years of experience in corporate finance, FP&A, Treasury, investment banking or other related fields, your level of English is intermediate, you have an advanced Excel level, you have excellent Ability to relate, you communicate assertively and you know how to manage your time to meet the proposed goals and objectives, join our team! You can work remotely, with a salary allocation of USD 1,500.

For further information, please contact us at

¡Te estamos buscando!

Si eres profesional graduado en áreas administrativas o financieras, tienes de 2 a 3 años de experiencia en Finanzas corporativas, FP&A, Tesorería, banca de inversión u otros campos relacionados, tu nivel de inglés es intermedio, tienes un nivel de Excel avanzado, posees excelente habilidad para relacionarte, te comunicas de manera asertiva y sabes gestionar tu tiempo para cumplir con las metas y objetivos propuestos, ¡únete a nuestro equipo!, puedes trabajar de manera remota, con una asignación salarial de USD 1.500.

Para obtener más información, comuníquese con nosotros en

 Digital HR Communications Specialist

We are looking for professionals like you!

Professional in Communications, Psychology, Administration or related areas. Desirable Master in Organizational Communication, Human Resources or similar. With more than two years of experience in communication areas (internal and/or external) and/or HR processes (culture, engagement, Employer Brand), managing external suppliers such as advertising or marketing agencies. It is desirable that they have knowledge and experience in project management, leading communications, and/or HR Projects. Advanced English level, computer skills developed for the use of Microsoft Word, Excel, and PowerPoint, and preferably in other communication and design tools. Geographic location open to any country in Latin America, desirable Colombia or Panama.

For further information, please contact us at

¡Nos encontramos en búsqueda de profesionales como tú!

Profesional en Comunicaciones, Psicología, Administración o áreas afines. Deseable Maestría en Comunicación Organizacional, Recursos Humanos o similares. Con experiencia de más de 2 años en áreas de comunicación (internas y / o externas) y / o procesos de RR.HH (cultura, engagement, Employer Brand), manejo de proveedores externos  como agencias de publicidad o marketing. Deseable que posea conocimiento y experiencia en gestión de proyectos, liderando comunicaciones y / o Proyectos de RRHH. Nivel de inglés Avanzado, habilidades informáticas desarrolladas para el uso de Microsoft Word, Excel y PowerPoint, y preferible en otras herramientas de comunicación y diseño. Ubicación: geográfica abierta a cualquier país en Latinoamérica, deseable Colombia o Panamá.

Para obtener más información, comuníquese con nosotros en

By filling in an application form you give VaxTrials permission to keep your personal data stored for one year after the termination of the application procedure. We may use it to contact you about possible future vacancies. You can contact us at any time to view, change or delete your Curriculum Vitae. We will not share your data with third parties.

Stay connected! When new positions open up, or if we start accepting open applications for our talent pool again, we offer the possibility to keep your CV in our data base.

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