Requires a Ph.D. or M.S. in pharmacology, toxicology, or closely related discipline, or DVM and a minimum of 2 years of relevant experience. CRO experience and DABT or DSP are preferred.
Job Requirements/Core Requirements
Exhibit excellent communication, interpersonal and technical writing skills.
Study direction of GLP general toxicology, safety pharmacology or genetic toxicology studies
Working knowledge of GLP requirements and various international regulatory guidance relevant to drug development.
Initiate, monitor, and oversee studies.
Interpret study results and author study reports.
Maintain knowledge of study types used to support drug safety assessments.
Maintain and facilitate communication with sponsors and management
Serve as a Study Director for GLP and non-GLP studies, interpret data and integrate results into the main study report
Provide scientific contribution.
Facilitate projects to meet client program milestones
Perform activities in compliance with GLPs and departmental Standard Operating Procedures (SOPs).
Maintain Personal Documentation Record
(curriculum vitae, job description, and training record)
Facilitate cooperation between departments.
Identify and develop new business ventures.
Adhere to corporate Environmental and Occupational Safety policies.
Ability to work with minimal supervision.
Provide status updates to account managers, clients and management
We offer a competitive salary along with a comprehensive benefit plan.