Senior CRA to manage 2–3 clinical trials and site management activities.
Conduct on-site and remote monitoring with diverse studies for CRO clients.
Permanent, fully remote position; travel to investigative sites as needed.
Requirements include experience with oncology and complex trials; strong GCP/ICH knowledge.

🎯 Requirements

University Degree in scientific, medical or paramedical disciplines.
8+ years of clinical research experience; CRA onsite monitoring experience.
Experience with oncology, respiratory and complex trials.
Strong knowledge of clinical trial operations, GCP/ICH and regulatory requirements.
Fluent in English and local language(s); MS Office proficiency; willingness to travel.

🎁 Benefits

Remote working opportunity.
Global CRO with 28+ years of experience and 4,000+ professionals.
Opportunities for training and professional development.

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