Remote job · Management

Freelance Clinical Research Associate

Remote (Portugal)
A mid-size contract research organisation
Posted 13 Oct 2026

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About the role

A part-time freelance monitoring role supporting clinical trials in internal medicine and neuroscience, covering site initiation, monitoring and close out in line with regulations and sponsor procedures.

What you will do

Monitor trial sites on site and remotely according to sponsor and company procedures, GCP and ICH guidelines
Assess subject safety, data integrity and quality through required monitoring activities
Check informed consent and protocol compliance to protect study participants
Review case report forms and source documents for validity and accuracy
Verify accountability and management of investigational products
Report visit findings and corrective actions promptly and escalate deficiencies

What they look for

One to three years of relevant clinical experience or academic background in trials
Experience in urology or overactive bladder
Understanding of Good Clinical Practice and ICH guidelines
Fluent English and Portuguese
Strong organisation, communication and computer skills

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