Remotely
leadershipgcponcologypharmacovigilanceclinical developmentregulatoryclinical study reports
Job Description
📋 Description
- Lead design, execution, and interpretation of clinical trials across programs.
- Own cross-functional teams to deliver high-quality clinical data.
- Oversee study teams, timelines, and data safety assessment.
- Lead regulatory interactions and ensure GCP compliance.
- Contribute to translational strategies and due diligence as needed.
🎯 Requirements
- MD/DO or equivalent with oncology subspecialty desirable.
- 5+ years in clinical development; 7+ preferred.
- Proven leadership in cross-functional global teams.
- Strong knowledge of trial methodology and regulatory requirements.
- Ability to interact with external partners and internal stakeholders.
- Experience in study protocol design and regulatory submissions.
🎁 Benefits
- Competitive compensation with annualized range based on location.
- Comprehensive benefits package and long-term incentive programs.
- Equal opportunity employer; includes veterans and disabled.
- Participation in 401(k) and related employee programs.