Reporting Associate Preclinical Studies
| Company | LabCorp |
|---|---|
| Location | Greenfield, IN, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Bachelor’s |
| Experience Level | Junior, Mid Level |
Requirements
- BS Degree in life science area such as Biology or related area, related experience may qualify in lieu of education.
- Strong knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)
Responsibilities
- Prepares the study report using details described in the protocol, protocol amendments, and study communications and Covance or client-specific requirements
- Incorporates contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report
- Conducts direct contact with clients, prepares form letters and communication text
- Addresses quality assurance inspection items on GLP-regulated studies
- Finalizes study reports and obtain, prepare, and deliver materials to archives and prepares report amendments
- Prepares data tables including completing basic statistical analysis in table generation programs. Assists in the preparation of tabulated summaries in association with the study director. Performs quality check data tables that were manually prepared, overall reviews data tables for accuracy
- Schedule and organize client site visits and client conference calls
- Prepares reports and scheduling tasks. Identifies and resolves changes to established study schedules to ensure client deliverables are met.
- Prepares study reports, prepares and delivering presentation, participating in staff meetings, participating in process improvement projects, and/or liaising with cross-site staff.
- Reviews and adjust the reporting schedule to ensure client expectations are met.
- Schedules and leads the prewriting meeting, as required Schedules and coordinates study report finalization efforts.
- Coordinate expedited reporting, as necessary, among global counterpart
Preferred Qualifications
- 1 year of experience in science, technical writing, and/or document production/publishing in scientific field preferred but not required.
- 1 year of technical writing or data tabulation experience, especially in pharmaceutical research or life sciences preferred but not required.