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SciPro · Carlsbad, California
Toxicology Study Coordinator
Facilitation of study contracts (SOWs), protocols, reports, etc.
Test article and formulation requests, review of study protocols, reports, amendments, etc
Track and maintain study specific milestones using in-house database in support of quarterly finance updates
Coordinate sample shipments, receipt and transfer of sensitive study samples; maintain Chain of Custody
Prepare, review and distribute data templates
Maintain and update study outlines templates
General assistance to Scientists will be an essential part of the role and additional non study specific support may be required across departments
QC reports, data, data tables, presentations, documents for regulatory submissions (eg IND, IB, NDA, etc) using advanced functions of MS Word, Excel and e-sub compliance software, as appropriate.
Plan, prioritize, and manage a diverse workload with associated responsibilities
Schedule and participates in department and study-related meetings, as required, prepare meeting minutes.
A Bachelor’s degree in biology or a related science field is required along with a minimum of 5 years relevant experience. Experience in nonclinical study conduct is required.
Strong candidates must be highly proficient with Microsoft Office applications, possess excellent organizational, multitasking, and communication skills. The ability to work both independently and collaboratively is essential. The ideal candidate will also demonstrate flexibility and adaptability in a dynamic, team-oriented environment.
Details
| Company | SciPro |
| Location | Carlsbad, California |
| Type | FULL TIME |
| Niche | Full-time |