Amie Carter Email & Phone Number

Responsible for the leadership and direction of projects within the clinical animal health division.

Mattawan, Michigan, United States

Responsible for leadership and direction of Quality Assurance functions while ensuring quality and compliance in activities including, but not limited to: scheduling, consultation, observation resolution, training, review of events/investigations, generating metrics and report data trending, interviews/recruiting, and SOP reviews. Assisted in sponsor.

Mattawan, MI

Supervisory responsibilities while providing leadership and direction to auditors. Serves as resource to sponsors and internal customers as well as assisting with Sponsor visits, Sponsor audit report responses, and coordination of subcontractor audits. Provides input to management on development of department goals and resources.

Mattawan, MI

Study/Project team:Assured GLP compliance of facilities/sites, including regulated studies & projects, and reporting results of these functions to management. Performed assessment of protocols, system validation records, system use, laboratory procedures, equipment records, training records, data, and reports to determine the level of compliance with.

Everett, WA

Coordinated auditing activities to ensure compliance with SOPs and GLP requirements. Performed a wide variety of activities pertaining to assuring compliance with applicable regulatory requirements by conducting audits, inspections, data and documentation reviews.

Supported activities of contract research organizations and clinical research coordinators. Applied technical skill and knowledge of regulatory standards and expectations to establish and promote best practices.

Managed all aspects pertaining to the conduct of clinical and non-clinical research studies in companion animal immunology within core project teams with thorough understanding of study report and protocol, GLP, GCP, EMEA, and OECD requirements and actively promoted best practices based on knowledge of those requirements.

Responsible for the design, implementation and reporting of GCP, GLP, and non-GLP Developmental and Reproductive toxicology studies conducted on and off-site at contract facilities.

Conducted acute, sub-chronic, and chronic general and reproductive toxicity studies, postnatal behavioral, developmental, functional, and/or neuropharmacological examinations of laboratory animals in a GLP environment.