North AmericaFull TimeOperations
Remotely
gcpregulatorysopipcapactmsetmf
Job Description
📋 Description
- Lead planning, conduct and oversight of clinical studies per SOPs and ICH-GCP
- Primary client contact; manage monthly invoicing and budget variance
- Develop study documents and training materials; support Investigator Meetings
- Lead site feasibility, recruitment strategy and KPI/metrics reporting
- Oversee IP management, IP release, audits and CAPA implementation
- Manage cross-functional teams and vendor relationships
🎯 Requirements
- Bachelor’s degree in science or health-related field; advanced degree preferred
- Minimum 7 years clinical research experience with significant monitoring
- Excellent communication, organization, and interpersonal skills
- Ability to travel domestically and internationally
🎁 Benefits
- Discretionary annual bonus
- Health insurance
- Retirement savings benefits
- Life and disability insurance
- Parental leave and paid time off