Senior Clinical Trials Monitor & Site Liaison

Terumo Medical Corporation; New Jersey; On-site; USD 110,000 - 150,000; Full time

Job summary

Terumo Medical Corporation seeks a Senior Clinical Research Associate to support daily trial operations, monitor multiple sites, and ensure data integrity and protocol adherence. The role serves as the liaison between investigators and Terumo, handling site training, regulatory document collection, enrollment tracking and CRF verification against source documents.

The Sr. CRA will contribute to development of procedures and templates to improve quality and optimize clinical study processes

Qualifications

• BS/BA or higher in a clinical or scientific area; RN preferred.
• Minimum of 5 years experience independently monitoring clinical trials; medical device preferred.

Responsibilities

• Monitor multiple clinical trial sites and studies.
• Ensure adherence to protocol, GCP and all regulations.
• Train sites and collect regulatory documents.
• Track enrollment and verify CRFs against source documents.
• Communicate findings to CRA Manager and PM.

Skills

Clinical trial monitoring

Regulatory knowledge

GCP compliance

Site management

Communication

Education

BS/BA in clinical or scientific field

RN preferred

Tools

CTMS

Job description

Terumo Medical Corporation seeks a Senior Clinical Research Associate to support daily trial operations, monitor multiple sites, and ensure data integrity and protocol adherence. The role serves as the liaison between investigators and Terumo, handling site training, regulatory document collection, enrollment tracking and CRF verification against source documents.

The Sr. CRA will contribute to development of procedures and templates to improve quality and optimize clinical study processes