Senior Clinical Scientist, Oncology

📋 Description

• Develop study concepts, designs, endpoints; align with leadership.
• Contribute to protocol drafting; respond to health authority feedback.
• Provide protocol trainings to internal and CRO teams.
• Design CRFs; ensure alignment with study requirements.
• Oversee real-time data reviews; coordinate with CROs as needed.
• Represent clinical science in meetings; prepare presentations.

🎯 Requirements

• PhD/RN/MS required.
• 5-8 years as Clinical Scientist; oncology preferred.
• Experience with randomized controlled trials preferred.
• Experience with project management, clinical research, scientific writing.
• Travel ~15-20% domestically and internationally.
• HIPAA/PHI privacy training within 30 days; maintain status.

🎁 Benefits

• Annual performance incentive bonus
• Long-term equity awards
• Comprehensive health benefits (medical, dental, vision)
• 401(k) with company match
• Generous paid time off and holidays
• Additional wellness and work-life benefits