Manage clinical elements within a trial across multiple sites
Oversee site selection, start-up, enrolment, monitoring, data cleaning, close-out
Ensure timely delivery of trial milestones and high quality
Coordinate regulatory docs and ongoing oversight with cross-functional teams
Mentor and train team members
Identify risks to timelines and propose action plans

🎯 Requirements

Bachelor's degree in science/health or related field (oncology experience)
Multicountry clinical lead experience in CRO/Pharma/Biotech
Extensive oncology trial management experience
GCP/ICH knowledge and clinical development process
Travel domestically and internationally; English fluency
Proficiency with CTMS, eTMF, EDC, IXRS; MS Project/Office

🎁 Benefits

Remote work options across several European countries
Grow within a specialized precision medicine CRO
Work with multidisciplinary teams in oncology and rare diseases
Opportunity for international travel
Equal Opportunity Employer

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