Scientific Director I, Oncology Clinical Development
$160,500–$305,000 year
Hybrid · North Chicago, Illinois, United States
Job Summary
Scientific Director I, Oncology Clinical Development: oversees the direction, planning, execution and interpretation of clinical trials within a clinical development program. Under supervision, designs and implements study protocols and educates investigators and study staff. Responsible for review and communication of safety and efficacy data, potential oversight of enrollment timelines, and contribution to regulatory submissions and clinical study reports. Collaborates across Medical Affairs, Commercial and other functions; stays current with scientific literature and conferences to augment expertise. Requires ability to interpret regulatory requirements and ensure Good Clinical Practices and pharmacovigilance standards are followed. Strong cross-functional collaboration and communication skills are essential; advanced degree preferred.
Required Qualifications
- Bachelor's degree in the sciences; advanced degree (e.g., MS, PhD) preferred.
- Experience in clinical trial design, regulatory compliance, and cross-functional collaboration.
- Knowledge of clinical trial methodology and regulatory requirements.
- Excellent oral and written English communication skills.
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