North AmericaFull TimeOperations
Remotely
excelgcpsite managementcromonitoringgood clinical practicesmartsheetich e6(r3)
Job Description
📋 Description
- Reporting to the Sr. Director, Clinical Operations, collaborates within Clinical Operations to
- Partner with Clinical Operations Study Lead and cross-functional team to support studies from
- Lead operational management for assigned regions and sites; monitor performance metrics, mitigate
- Serve as primary sponsor contact for investigators and sites; build relationships and resolve
- Lead vendor management for CROs and other vendors (IRT, imaging, labs); set expectations, ensure
- Oversee CRO monitors; review monitoring docs, evaluate performance, co-monitoring as needed
🎯 Requirements
- Bachelor’s degree or equivalent training/experience (RN/PA, BSN). Minimum 4-6 years of clinical
- Experience supporting global studies in fast-paced settings; success working with CROs and vendors.
- Excellent communication skills; ability to meet milestones in a team. Able to collaborate remotely.
- Experience within biotechnology or pharmaceutical sponsor organizations; site initiation, interim
- MS Office (Excel, Word, PowerPoint) and SmartSheet proficiency.
🎁 Benefits
- Market-leading compensation
- 401(k) with employer match
- Flexible, hybrid/remote work options; hybrid work model with some in-office days
- Comprehensive health coverage; 100% employer-paid premiums for medical, dental, vision
- Comprehensive PTO; paid holidays; fertility/family-forming benefits; HSA and FSA options
- Career development pathways; education resources and coaching
