- Maple Grove, Minnesota, United States
- Senior
- 4–6 years
Lead and manage clinical research operations, including TMF management, payments, contract administration, and process improvements across multiple studies.
Responsibilities
- Develop and monitor study operational metrics and compliance risks
- Collaborate with study teams to mitigate risks
- Lead end‑to‑end TMF strategy and execution
- Oversee department payment processes and compliance
- Manage administration and timelines for clinical, vendor/CRO, and consultant agreements
Requirements
- Bachelor's degree in Life Sciences, Health Sciences, Business Administration, or related field
- Nice to have: medical device
- Nice to have: pharmaceutical
- Nice to have: biotechnology