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Clinical Trial Specialist
1 week ago
We are seeking a skilled professional to join our team as a Clinical Trial Specialist. As a key member of our clinical development department, you will be responsible for providing clinical trial capabilities in support of our research efforts.
Your primary focus will be on ensuring that investigator sites meet the necessary requirements to enroll study participants into clinical trials from a budgets and contracts perspective.
You will work closely with site personnel, service providers, and internal teams to initiate and maintain clinical trial activities, ensuring compliance with local and regional regulations, data privacy requirements, and Lilly quality standards.
In this role, you will communicate directly with sites to facilitate start-up and ongoing collaboration regarding budgets and contracts activities during maintenance and close-out.
You will also identify, communicate, and resolve issues related to budgets and contracts, while incorporating country-specific regulatory and data privacy requirements into budget and contract documents.
Key responsibilities include collecting and administering financial data from contracting partners and vendors, ensuring finance-specific requirements are administered in budget and contract documents, and supporting payment processes.
To succeed in this role, you will possess effective communication, negotiation, and problem-solving skills, as well as language capabilities in Romanian and English.