Scientist

Frontage Laboratories•Concord Township, OH

17h

About The Position

We are seeking a detail-oriented and highly collaborative Scientist to act as a Study Director for in vivo toxicity and PK/TK studies. The successful candidate will direct these studies to ensure project timelines are met, and effectively communicate with project managers, clients, and internal teams.

Requirements

B.S. in Toxicology, Pharmacology or related scientific discipline with a minimum of 2 years of CRO or pharmaceutical experience.
Excellent communication, interpersonal, and technical writing skills.
Understanding of common in vivo toxicological study endpoints
Ability to organize and clearly present complex data and concepts
Ability to work on multiple projects at the same time
Understanding of GLP requirements
Ability to successfully independently and corroboratively in a team environment

Responsibilities

Study direction of in vivo non-GLP and GLP general toxicology and PK/TK studies.
Initiate, monitor and oversee studies
Interpret experimental data
Author study protocols and reports.
Acts as a primary point of study contact
Maintain schedule of projects and timelines to meet client program milestones
Maintain the proper level of regulatory compliance for each study and addressing QA audit findings
Maintain and facilitate communication with sponsors and management
Help with training and/or mentoring of junior scientific staff.
Follow Standard Operating Procedures (SOPs), Good Laboratory Practices (GLPs), Health & Safety standards and department policies/procedures in the performance of all duties.
Work with support teams including sample management, vivarium, QC, RW, PM & QA, BD as well as PIs and management.
Other duties as assigned.