Our client is a respected expert consulting firm which operates globally, primarily in the chemical registration and defense realm. Their clients include individual companies and consortia.
As a result of increased toxicology testing and emerging regulations, the company is seeking a person to manage external testing programs on behalf of clients. The person hired for this role will monitor studies and/or perform quality assurance for nonclinical GLP and non-GLP studies and laboratories. He/She will also assess the resulting scientific data for compliance with applicable guidelines and regulations.
The VP of Scientific Affairs to whom the job reports would like to hire a graduate degreed scientist (toxicology or an allied science) with a few years of experience relevant to product safety/development. A person who has worked as a Study Director and now looking for a career transition would be ideal. Verbal and written communication skills are paramount.
Growth opportunities within the company, in the regulatory toxicology realm, are available.
The company is fully supportive of a remote work arrangement. The travel associated with the position will be reasonable.
Search assignment #1534