The Associate Principal Scientist role is designed to support the regulatory approval of new companion animal and livestock products by designing, coordinating, monitoring, and reporting on clinical laboratory and field studies.
Requirements
- Understanding of GCP Good Clinical Practices guidelines.
- GLP Regulations
- Good Clinical Practice (GCP)
- Biomarker Assay Development
- Clinical Research
- Clinical Sciences
- Clinical Study Design
Responsibilities
- Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet scientific and regulatory requirements by the setting of objectives, budget, resources, timelines, and the study protocol/related documentation.
- Plan and coordinate the monitoring and data management activities of each study.
- Ensure that the study is conducted according to legal requirements, GCP, and the applicable internal policies and procedures.
- Prepare the Final Study Report
- Assume responsibility for certain monitoring and data management tasks (e.g., User Acceptance Test of electronic CRFs)
- Monitor clinical studies under the leadership of other Scientists.
- Conduct quality control inspections of study protocol, study documentation files and reports.
Other
- Doctor of Veterinary Medicine, OR equivalent veterinary degree
- Four years in clinical research or similar research role.
- Experience in a clinical study related role.
- Principled verbal and written communications
- Travel Requirements: 25%
