Global Clinical Research Associate | Remote-Friendly Travel

Alira Health; Boston (MA); Híbrido; USD 70.000 - 95.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Professional development

Global travel

Flexible work programs

Descripción de la vacante

Alira Health is seeking a Clinical Research Associate (CRA) to join our global clinical team in the Boston area. The CRA will conduct site monitoring for clinical trials, provide oversight and guidance, and ensure protocol compliance with ICH GCP and sponsor SOPs.

Collaboration with Lead CRAs, project managers, and other functions is essential to address site questions and training needs. The role involves coordinating site visits, budget considerations, and data integrity via source document

Formación

• BS in Biology or Life Sciences, or equivalent.
• Experience with clinical trial monitoring and ICH GCP.
• Ability to establish positive sponsor, site and team relationships.
• Able to autonomously manage monitoring activities.

Responsabilidades

• Provide guidance and oversight to CRA team to meet scope, SOPs, timelines and budget.
• Review monitoring visit reports and conduct co-monitoring visits as needed.
• Ensure investigator site visits are timely and compliant.
• Coordinate with cross-functional departments for issue resolution.
• Develop study-specific Monitoring Plans and training materials.

Conocimientos

Attention to detail

Organizational skills

Leadership

Communication

Problem solving

Travel ability

Educación

BS in Biology

BS in Life Sciences

Herramientas

CTMS

EDC

Descripción del empleo

Alira Health is seeking a Clinical Research Associate (CRA) to join our global clinical team in the Boston area. The CRA will conduct site monitoring for clinical trials, provide oversight and guidance, and ensure protocol compliance with ICH GCP and sponsor SOPs.

Collaboration with Lead CRAs, project managers, and other functions is essential to address site questions and training needs. The role involves coordinating site visits, budget considerations, and data integrity via source document