Clinical Trials Specialist – Cardiac Device Validation

Acorai AB; Viseu; On-site; EUR 38,000 - 56,000; Full time

Job summary

Acorai AB in Portugal is seeking a hands-on clinical research professional to run multicentre investigations validating the SAVE Sensor System. You will coordinate between sites, data, and regulatory requirements to ensure protocol compliance and high-quality evidence.

You will design e CRFs, manage data, monitor site activities, prepare datasets, oversee ethics submissions, and contribute to regulatory submissions as part of the Clinical Trials Specialist role for Cardiac Device Validation in

Qualifications

• Hands-on clinical research professional experience.
• Experience coordinating multicentre investigations.
• Knowledge of ethics submissions and regulatory processes.

Responsibilities

• Coordinate between sites, data, and regulatory requirements to ensure protocol compliance and high-quality evidence.
• Design electronic case report forms (eCRFs) and manage data workflows.
• Monitor site activities and data quality across multicentre investigations.
• Prepare datasets and contribute to ethical submissions and regulatory filings.

Skills

Clinical research coordination

Data management

Regulatory compliance

eCRF design

Site monitoring

Job description

Acorai AB in Portugal seeks a hands-on clinical research professional to run multicentre investigations validating the SAVE Sensor System. You will coordinate between sites, data, and regulatory requirements to ensure protocol compliance and high-quality evidence. You will design e CRFs, manage data, monitor site activities, prepare datasets, oversee ethics submissions, and contribute to regulatory submissions.

Clinical Trials Specialist – Cardiac Device Validation Portalegre, Portuguese Republic, PT