Monitor progress of clinical studies at investigative sites per protocol and ICH-GCP.
Coordinate site setup and monitoring: identify investigators, regulatory submissions, visits.
Travel up to 50-60%; some roles require international travel.
Work in a smaller CRO with direct line management support.
Focus on 1-2 studies and develop protocol expertise.

🎯 Requirements

Graduate or postgraduate degree in a scientific or healthcare discipline.
2.5+ years as a CRA in CRO or pharma; site management exp.
Excellent communication and organizational skills; team player.
Evidence of a client-focused approach.
Availability for domestic travel up to 50-60%; may include international travel.
Fluency in English and local language of country where position based.

🎁 Benefits

Discretionary annual bonus.
Private medical insurance.
MultiSport Card.
Life insurance.
Pension.
Home working allowance.

Apply on employer's website

This employer gathers applications via their own applicant tracking system.

You will be redirected to an external application form.

Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Healthcare Jobs. Just set your preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.

Activate JobCopilot