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informed consent regulatory cro phi hipaa📋 Description
- Implement trial activities per protocol with sites and CROs.
- Manage and coach clinical research staff.
- Oversee vendor contracting, budgets, and payments.
- Design study documents: protocol, ICFs, CRFs, binders.
- Train CROs, vendors, investigators, and coordinators.
- Monitor trial progress and report status to stakeholders.
🎯 Requirements
- Bachelor’s degree in life sciences; advanced degree preferred.
- 5-10 years clinical research; 3-5 years leading trials.
- 2+ years staff management; CRO management preferred.
- Experience independently managing design, protocol, monitoring, recruitment.
- Familiar with clinical research regulations.
- Proficiency in MS Word, Excel, PowerPoint; strong organization.
🎁 Benefits
- Comprehensive medical, dental, vision, life, disability benefits.
- Free testing for employees and immediate family; fertility care benefits.
- Pregnancy/baby bonding leave; 401k; commuter benefits.
- Employee referral program.
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