Related skills
forecasting vendor management regulatory submissions ich-gcp cro management📋 Description
- Lead overall management of multiple clinical trials from Phase II–III.
- Ensure adherence to ICH-GCP, SOPs, and regulatory guidelines.
- Oversee CROs and vendors to meet milestones and quality.
- Communicate project status to stakeholders and escalate issues.
- Plan budgets, timelines, and risk mitigation across programs.
🎯 Requirements
- BA/BS in life sciences or equivalent.
- 8+ years clinical research experience.
- 3+ years leading global projects.
- 2+ years Biotech industry preferred.
- Knowledge of pharma processes and regulatory frameworks.
- Strong cross-functional leadership and communication.
- Experience budgeting and managing program-level budgets.
🎁 Benefits
- Salary range: $180,000 - $195,000 per year.
- Base pay, bonus, equity grant opportunities.
- Health, welfare, and retirement benefits.
- Three weeks PTO, two shutdown weeks, paid sick leave.
- Professional development resources and growth.
Meet JobCopilot: Your Personal AI Job Hunter
Automatically Apply to Operations Jobs. Just set your
preferences and Job Copilot will do the rest — finding, filtering, and applying while you focus on what matters.
Help us maintain the quality of jobs posted on Empllo!
Is this position not a remote job?
Let us know!