Related skills
ms office powerpoint edc ms project etmf📋 Description
- Manage clinical elements: site start-up, enrolment, monitoring, and data cleaning.
- Deliver trials on time and ensure all trial deliverables are met.
- Maintain regulatory docs and oversee study activities with cross-functional teams.
- Mentor and train team members.
- Identify timeline risks and propose action plans to sponsors.
- Lead CRAs to build site relationships for monitoring, regulatory, IP, and payments.
🎯 Requirements
- Bachelor's degree or equivalent in science/health field; oncology experience preferred.
- Proven experience leading clinical trials across multiple countries in CRO/Pharma/Biotech.
- Significant oncology trial management experience.
- Strong knowledge of GCP/ICH guidelines and clinical development process.
- Availability for domestic and international travel; English proficiency.
- Proficient with CTMS, eTMF, EDC, IXRS, MS Office.
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Operations Jobs. Just set your
preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!