Clinical Trials Specialist – Cardiac Device Validation

Acorai AB; Portugal; On-site; EUR 60,000 - 80,000; Full time

Job summary

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 eCRFs, manage data, monitor site activities, prepare datasets, oversee ethics submissions, and contribute to regulatory submissions.

Qualifications

• Bachelor's degree or higher in life sciences or related field.
• 3+ years in clinical research (CRA, study nurse/coordinator, or clinical data manager).
• Working knowledge of ISO 14155 and ICH GCP.

Responsibilities

• Design and maintain eCRFs and data management plans.
• Run data review, query management, and reconcile device data with reference data.
• Conduct site initiation, monitoring and close-out visits (on-site and remote).
• Prepare datasets for analysis and support database lock.
• Prepare ethics committee and IRB submissions and contribute to regulatory submissions.
• Maintain an inspection-ready Trial Master File and keep study documentation up to date.

Skills

Clinical research

Data management

Site monitoring

Travel readiness

Education

Bachelor's degree in life sciences or related field

Tools

Viedoc

REDCap

Medidata Rave

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 eCRFs, manage data, monitor site activities, prepare datasets, oversee ethics submissions, and contribute to regulatory submissions.