International Careers

Associado de Pesquisa Clínica Contratado(a)

• Graduação ou experiência.

• Mínimo de 5 anos de experiência como CRA.

• Proficiência em inglês escrito e falado é necessária.

• Experiência prévia em monitoramento de estudos oncológicos é preferencial.

• Ter bom desempenho em uma função com alta disponibilidade para viagens, com disponibilidade de até 70%.

Asociado de Investigación Clínica por Contrato

• Licenciatura o experiencia.

• Mínimo de 5 años de experiencia como CRA.

• Se requiere dominio del idioma inglés escrito y hablado.

• Se prefiere experiencia previa en el monitoreo de estudios de Oncología.

• Destacar en un puesto con muchos viajes, con disponibilidad de hasta el 70%.

Attaché(e) principal(e) de recherche clinique

• Diplôme de licence ou expérience équivalente.

• Minimum de 5 ans d’expérience en tant que CRA.

• Maîtrise requise de l’anglais écrit et oral.

• Une expérience préalable dans la surveillance d’études en oncologie est souhaitée.

• S’épanouir dans un poste impliquant de nombreux déplacements, avec une disponibilité allant jusqu’à 70 %.

Current Openings

Requirements:

Bachelor’s degree or equivalent combination of education and clinical research experience.
Minimum of 5 years monitoring experience.
Previous experience monitoring Oncology clinical trials.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Excellent organizational and communication skills, with strong attention to detail.
Ability to travel.

Requirements:

Bachelor’s degree or equivalent combination of education and clinical research experience.
Minimum of 5 years monitoring experience.
Previous experience monitoring Oncology studies required.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Excellent organizational and communication skills, with strong attention to detail.
Experience managing complex projects.
Thrive in a high-travel role, with availability up to 70%.

Requirements:

Bachelor’s degree or equivalent combination of education and clinical research experience.
Minimum of 5 years monitoring experience.
Previous experience monitoring Oncology studies required.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Excellent organizational and communication skills, with strong attention to detail.
Experience managing complex projects.
Thrive in a high-travel role, with availability up to 70%.