Clinical Research Scientist - Companion Animal Development

The Company is a global research-based company that develops and delivers product and services to enhance animal health and production.  We value innovation, both in scientific research and daily operations, and strive to cultivate a collaborative work environment for more than 1,000 employees worldwide.  Founded in 1954, The Company is a division of a $25B pharma company out of the Midwest.   

KEY OBJECTIVES/DELIVERABLES:

• Coordinate, supervise and/or conduct effectiveness, toxicology, safety and bioanalytical studies. Experienced/first-hand knowledge in clinical effectiveness trial conduct (lab and client-owned/field) and the protocol concurrence process w/CVM & other Regulatory Agencies. Knowledgeable in conduct of safety, toxicological & bioanalytical studies.
• Design/Develop study protocols, data capture forms, data output, and reports.
• Coordinate, supervise and/or conduct data management, statistics, and monitoring activities as necessary.
• Identify and select CROs and establish contract agreements, and maintain a positive business collaboration.
• Effectively collaborate with a cross-functional development team to develop and register new Companion Animal molecules.
• Compliance: Follow appropriate standard operating procedures to ensure compliance with applicable regulatory requirements and corporate quality standards.

• Previous experience conducting multiple parallel studies in animals.
• Previous experience with documentation and conducting research in a regulated environment (GLP, GCP).
• Previous experience working with external contract research organizations.
• Leadership: Proactively search for solutions.
• Work effectively and flexibly within and across all The Company R&D teams and external collaborators to achieve overall The Company R&D deliverables.
• Create a positive work environment that is aligned with company objectives.
• Provide and accept challenge to deliver innovative technical solutions and create an innovative culture.
• Qualified candidate must be legally authorized to be employed in the United States. The Company does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this position.

Clinical-Research-Scientist-Medallion.pdf