Trial Activation Approval Specialist I Position Available In Mecklenburg, North Carolina
Tallo's Job Summary: The Trial Activation Approval Specialist I role involves facilitating site start-up, ensuring timely approval, and collaborating with internal and external teams. Responsibilities include collecting and reviewing essential documents, identifying activation delays, and improving SSU metrics. The position requires working closely with Study Startup and Clinical Operations teams. The salary and recruiting details are not specified in the job description.
Job Description
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Facilitate site start-up and communication with internal and external team members to ensure flawless site approval and study timelines. Support sites and study teams to achieve rapid site start-up. Work directly with assigned sites on all essential document collection and review. Partner with internal Study Startup team, CROs, Clinical Operations teams, and TAU partners to improve overall SSU metrics and processes. Ensure standards are strictly applied to the SSU processes across projects. Review essential documents for start-up including ICF, FDF, 1572, CVs, etc. Quickly identify potential site activation delays and bring up to appropriate team members. Track actions and communications with sites to ensure timelines are met. Support resolving advanced issues identified by CROs and Clinical Operations teams in partnership with the internal Study Startup team. Review and provide feedback to management on site performance metrics. Ensure accuracy and completeness of the eTMF for assigned sites during start-up.
