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Associate Study Coordinator

1. Protocol Familiarization: Learn to read and comprehend study protocols, sample analysis outlines, amendments, and study schedules, ensuring understanding of regulatory requirements and Labcorp SOPs/P&Ps relevant to client deliverables.

2. Data Analysis and Reporting: Performs initial review of bioanalytical data and originates noncompartmental analysis (NCA) Phoenix WinNonlin in support of pharmacokinetic and toxicokinetic studies. Aids in report preparation, including tables and figures. Compiles analytical information from laboratory groups as required.

3. Documentation: Develop skills in preparing and proofing required paperwork for document and/or supply shipments, ensuring timely, efficient, and error-free processing.

4. Study Phase Scheduling: Assist in scheduling study phases in coordination with the Study Director/Principal Investigator, Schedulers and Lab Operations.

5. Quality Checking: Learn and successfully perform data, and report QC. Assist in checking protocols, proofing tables and figures prepared by others, ensuring proficiency with data collection systems and preparation software.

6. Coordination with Team: Work closely with other Study Coordinators (SCs) and Analytical Coordinators (ACs), Document Coordinators (DCs) to assist in preparing, monitoring, maintaining, and understanding finalization/archival, scheduling mechanisms for studies.

7. Study Archival: Perform tasks related to study archival, including notifying necessary personnel of study finalization/archival and gathering required paper/electronic items for archival purposes.

8. Other Duties: Undertake additional responsibilities as assigned by management.

Requirements:

Apply : https://careers.labcorp.com/global/en/job/2423317/Associate-Study-Coordinator

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