About This Role
We are seeking an experienced Study Manager to join our Clinical Trial Supply team. As a Study Manager, you will play a key role in managing the supply chain for clinical trials.
Key Responsibilities
* Manage the budget and costs associated with clinical trial supply
* Review invoices for accuracy and follow up with vendors as needed
* Track and process invoices within agreed timelines
* Allocate invoices and services according to cost structure
* Generate and maintain cost tracking reports for transparency and monitoring
* Maintain the Clinical Trial Supply budget and forecast sheets with planned and actual costs
* Develop and maintain an efficient filing structure for invoices to support teams
* Generate purchase orders for packaging materials and office supplies
* Support study teams with GCP compliant filing of clinical supply related study documents
* Process critical documents for CTS contracts, quality, and confidentiality agreements
Required Skills and Qualifications
* Bachelor's degree in life science, logistics, or project management
* At least 5 years of experience in clinical supply management or R&D project management
* Strong organizational and time management skills
* Good understanding of SAP and GMP, GCP, and GDP principles
Benefits
* Comprehensive compensation package
* Opportunities for career growth and development
* Collaborative and dynamic work environment