Global Clinical Research Associate

Alira Health Boston, LLC; Boston (MA); Hybrid; USD 85,000 - 115,000; Full time

Job summary

Alira Health Boston seeks a CRA to conduct site monitoring across clinical trials, ensuring protocol adherence and quality. The role involves collaboration with Lead CRAs, in-house teams, and sponsors to support study progress and training.

The position requires strong communication, adaptability, and knowledge of ICH GCP and FDA regulations, with travel to sites as needed. Competitive compensation offered.

Qualifications

• EU: Graduation in a scientific health field.
• Ability to establish and maintain positive relationships with Sponsor, Site and Project Team members.
• Ability to autonomously manage monitoring activities.

Responsibilities

• Provides guidance, oversight, and feedback to the CRA team to ensure adherence to scope, SOPs, timelines, and budget.
• Conducts site monitoring visits and co-monitoring as needed.
• Ensures investigator site visits are conducted timely and properly.
• Coordinates with cross-functional departments for issue resolution during monitoring.
• Assists in development of Monitoring Plans and training materials.
• Maintains site regulatory binder and ensures protocol compliance.
• Maintains QA of CRF data and source documents.
• Travels to study sites to support monitoring activities.

Skills

Attention to detail

Organizational skills

Analytical skills

Negotiation

Leadership

Communication skills

Team collaboration

Travel ability

Problem solving

Education

Bachelor of Science in Biology

Bachelor of Science in Life Sciences

Scientific health field degree

Certified Monitor (Italy CRO decree)

Tools

CTMS

EDC systems

Clinical trial databases

Job description

Alira Health Boston seeks a CRA to conduct site monitoring across clinical trials, ensuring protocol adherence and quality. The role involves collaboration with Lead CRAs, in-house teams, and sponsors to support study progress and training.

The position requires strong communication, adaptability, and knowledge of ICH GCP and FDA regulations, with travel to sites as needed. Competitive compensation offered.