Designs and executes livestock (cattle/swine) pharmaceutical/biopharmaceutical Clinical Development studies in compliance with US/CVM regulatory requirements. Deliver pilot and pivotal, clinical and non-clinical studies resulting in US NADA and ANADA approvals. Provides expertise in the areas of study conduct to livestock pharmaceutical research-phase projects.
Is responsible for overall conduct of clinical studies in support of Veterinary Medicine Research & Development (VMRD) livestock (cattle/swine) research and development projects, i.e. budgeting, investigator/site selection, protocol development/writing, monitoring, report writing.
Collaborate with Regulatory Affairs to gain concurrence for protocol approval and report/data submission with the Center for Veterinary Medicine (CVM). May also be involved in studies to support approvals in the EU or the rest of the world.
Collaborate with Clinical team to update the full project team with regards to study status, activities, timelines, outcomes, etc. Identify when resource, time, and/or budget constraints occur and work with the Project Manager and Project Team Leader to identify solutions.
Ensure that studies are conducted in compliance with applicable requirements, including Standard Operating Procedures (SOPs), corporate policies, and regulatory requirements and guidelines (e.g., Good Clinical Practice and Good Laboratory Practice).
EDUCATION AND EXPERIENCE
DVM/VMD with 3 years cumulative experience in either U.S. livestock (bovine and/or swine) production and/or private livestock practice experience and/or livestock pharmaceutical/biopharmaceutical product development experience
DVM/VMD with MSc and 3 years cumulative experience in either U.S. livestock production and/or private livestock practice experience and/or livestock pharmaceutical/biopharmaceutical product development experience
DVM/VMD with PhD in a livestock production-related discipline. Some experience in either U.S. livestock production and/or private livestock practice experience and/or livestock pharmaceutical/biopharmaceutical product development experience is desirable in addition to the PhD.
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact.
Zoetis is the leading animal health company, dedicated to supporting its customers and their businesses. Building on more than 60 years of experience in animal health, Zoetis discovers, develops, manufactures and markets veterinary vaccines and medicines, complemented by diagnostic products, genetic tests, biodevices and a range of services. Zoetis serves veterinarians, livestock producers and peo...ple who raise and care for farm and companion animals with sales of its products in more than 100 countries. In 2016, the company generated annual revenue of $4.9 billion with approximately 9,000 employees. For more information, visit www.zoetis.com