Обязанности и достижения:
Acting as Regional/Portfolio lead on allocated studies with active responsibility for the performance of the contract team assigned to the study
Successfully establishing CRO-Sponsor relationship on portfolio level with a new client, identifying risks and development areas, as well as creating a mitigation plan to resolve them.
Creating project-specific site contract documents, including study templates.
Facilitating clear communication, evaluation, and reporting of ongoing contract negotiations to study teams (e.g., Clinical Trial Management, Regulatory Submissions). This ensures that timelines are met, delays are effectively managed, and study team and Sponsor concerns are addressed.