Related skills
project management vendor management budgeting clinical research sops📋 Description
- Lead initiation, maintenance and close-out of multi-center studies.
- Ensure compliance with protocol, ICH-GCP, SOPs, and regulatory requirements.
- Plan and procure team resources to meet scope, budget, timeline.
- Develop study plans: project management, monitoring, risk, data and safety.
- Coordinate with central laboratories and external service providers/vendors.
- Manage site budgets, contracts, and change orders with sponsor.
🎯 Requirements
- Bachelor's degree in science, nursing, or biomedical field.
- Clinical research experience (CRA or Research Coordinator) preferred.
- Experience supporting business development: budgets, proposals, bid defense.
- Ability to work across multiple projects.
- Willingness to travel up to 30% (regional); travel flexibility.
- Excellent problem-solving and decision-making skills.
🎁 Benefits
- Equal Opportunity Employer.
- Values: Integrity, Trust, Teamwork, Respect.
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