Report Coordinator
3 hours ago
The individual in this role will support Scientists and Study Directors by reviewing data and preparing reports for Pharmacology and Toxicology studies. Key tasks will include data review, preparing report shells, writing report methods, figures, and tables using department specific software, and QC review, finalization and archival of reports. The individual in this role will have the opportunity to partner with Pharmacology, Toxicology and Operations staff to achieve the objectives of the role
Learn discovery pharmacology, safety pharmacology, and toxicology studies in order to prepare data and reports.
Learn to review protocols and reports using appropriate software.
Provides study support to contributing scientists/study directors/principal investigator by preparing report shells and writing report methods, inserting figures, and constructing tables with supervision.
May assist with protocol and protocol amendment documents.
Learns to use department specific software and equipment.
Learns to perform QC review of data, and reportables.
Learns to use department-specific software and equipment to write, format, finalize, and archive reports.
Work with others to train, ask questions as appropriate.
Communicate with internal clients to coordinate necessary study-related activities.
Learns the scope of a study and able to complete with mínimal supervision.
Builds positive relationships with internal clients.
Uses experience and knowledge to navigate study designs.
Recognizes changing situations and prioritizes and adapts accordingly.
Learns to acquire a full understanding of study requirements, GLPs, and how their role has implications in the overall project.
**Experience**:
2-3 years relevant scientific experience from previous role/employment
The Individual is expected to demonstrate a high level of technical ability
The Individual should demonstrate a consistent track record of high achievement.
**Education**:
**Labcorp is proud to be an Equal Opportunity Employer**:
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