Monitor studies at investigative sites per protocol and ICH-GCP.
Coordinate setup and monitoring activities (investigators, submissions, visits).
Travel up to 50-60% (domestic and international for some roles).
Be a protocol expert on 1-2 studies.
Maintain study quality and outcomes; address risks with solutions.
Collaborate with cross-functional teams and stakeholders.

🎯 Requirements

Graduate or postgraduate degree in scientific/healthcare field.
2.5+ years as CRA in CRO/pharma or equivalent.
Site management or equivalent clinical research experience.
Excellent communication and organizational skills; team player.
Travel up to 50-60%; international travel may be required.
Fluency in English and local language where position is based.

🎁 Benefits

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

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