Related skills
gcp edc clinical trials oncology cro📋 Description
- Lead cross-functional teams on complex clinical trials.
- Ensure delivery per contract, SOPs, ICH-GCP, and regs.
- Coordinate sponsor services: central labs, shipments, docs, etc.
- Oversee project development with Sponsor, Investigators, and team.
- Monitor milestones and quality across studies.
- Organize meetings and provide sponsor updates to stakeholders.
🎯 Requirements
- Bachelor's degree in scientific/medical disciplines.
- 8+ years in clinical research with project management.
- Oncology and respiratory study experience is required.
- Prior CRO experience required; CRA experience desirable.
- Knowledge of GCP/ICH and regulatory requirements.
- MS Office proficiency; EDC experience preferred.
- Fluent in English.
🎁 Benefits
- Permanent remote role with potential hybrid option.
- Global collaborative culture and work-life balance.
- Professional development and growth opportunities.
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