Sr Clinical Research Associate (Portugal)

Alimentiv · Lisboa

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Role summary

Senior Clinical Research Associate to oversee site monitoring services, ensure protocol and regulatory compliance, and serve as liaison between sponsors and investigative sites. Provides mentorship to junior CRAs and coordinates all clinical study execution activities.

What they're looking for

Extensive clinical research and site monitoring experience
Deep knowledge of ICH/GCP guidelines and local Portuguese regulations
Proven ability to mentor and develop junior clinical research staff
Strong regulatory compliance and protocol assessment expertise
Excellent cross-functional collaboration and stakeholder management skills

What you'll be doing

Oversee all aspects of clinical site monitoring and assess protocol compliance
Serve as primary contact between sponsors, Alimentiv, and investigative sites
Mentor and provide guidance to CRA I and II level staff members
Conduct CRA Assessment Visits and participate in audits and inspections
Coordinate study execution plans with cross-functional teams

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