Clinical Research Veterinarian

Clinical Research Veterinarian 

The scope of the position is to manage and direct all activities of the special techniques group in support of the conduct of global preclinical safety studies for pharmaceutical, OTC and medical device candidates.

Minimum Qualifications:

- Veterinarian (DVM) with laboratory animal medicine, veterinary surgery or ophthalmology experience
- Board certification by ACLAM, ACVS, or ACVO preferred
- At least 8 + years with supervisory and preclinical study implementation or conduct of ophthalmic procedures.
- Demonstrated clinical aptitude in surgical procedures required. Training opportunities available.

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Director – Clinical Development

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Manager – Pre-Clinical Development

The incumbent will formulate pre-clinical (target animal safety, toxicology and pharmacokinetic) development plans for new products in development and will work collaboratively within and across project teams to adhere to time schedules and meet critical deadlines. Read more

Manager of Clinical Development Projects

The primary responsibility of this role is to develop and execute comprehensive plans for products in clinical development. Key responsibilities include designing and writing study protocols, selecting veterinary investigators to execute clinical trials, overseeing and monitoring studies, and interpreting study results, writing study reports and preparing submissions to regulatory agencies. The position also provides technical support to commercial operations and presents results of studies to the scientific community.

Qualifications include a DVM and/or a PhD in an animal health related area. Preferred Qualifications include one or more years of experience in product development within or closely associated to the animal health pharmaceutical industry. Must possess the ability to organize and manage a variety of projects at any one time demonstrating attention to detail. Must possess good organizational skills and manage time efficiently. Must be self-motivated, possess good interpersonal skills and have the ability to lead and work within and across interdisciplinary teams. Travel is approx 25% within the United States. Limited international travel may be required.

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Veterinary Scientist

The primary role of the Veterinarian Scientist will be to improve human health by applying his/her veterinary surgical expertise and knowledge to the development of innovative medical devices. The role is uniquely situated to bring their practical experience to a cross-functional team including marketing, R&D, medical/clinical, and regulatory throughout the discovery, development and deployment phase. In these role the incumbent will influence project direction in order to bring the highest quality, superior and innovative products and procedures to market. The Veterinarian Scientist will be directly accountable for defining and executing the preclinical aspects of the product strategy. Read more

Manager – Regulatory Affairs

The position is responsible for coordinating quality regulatory submissions to the United States Department of Agriculture’s (USDA), specifically The Center of Veterinary Biologics (CVB), in order to meet company’s overall strategic and business objectives as products must first be licensed in the USA prior to licensing/marketing globally. Read more

Senior Scientist – Veterinary Biologics

This project leader is a highly technical position. The main responsibility is to independently develop and license new animal vaccines (viral only and viral/bacterial combination). The other responsibility is to assist Production and Quality Control in technical problem solving to support licensed products. Frequent communication and interaction with other groups such as Production, Quality Control, Registration and Quality Assurance is required.

Qualifications include MS in Virology/Microbiology/Biology, preferred PhD in Virology/Microbiology/Biology or DVM or related degree. Need 5 years experience in Veterinary biological R&D; direct USDA license experience.

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Director – Scientific Services

The incumbent will manage R&D scientific services for support of biological products and to ensure timely management of autogenous vaccines in R&D.  Coordinate, manage and communicate results of approved controlled and field trials, field safety trials and workflow of the Autogenous R&D Laboratory, workflow of Laboratory Services and Animal Services. 

Qualifications:  Ph.D and/or DVM, 5-10 years of experience managing controlled and field trials, 3-5 years experience managing a diagnostic laboratory, knowledge of modern poultry industry practices, familiarity with USDA regulations governing licensed and experimental biological products.

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Senior Regulatory Affairs Manager

The incumbent will provide leadership and direction by managing regulatory goals through interactions with Federal and State regulatory agencies to ensure all products receive regulatory approval, including post approval regulatory issues and provide input on strategic planning as related to regulatory issues.

Qualifications include advanced scientific degree (ex. DVM, PhD). 7-10 years in industry, 3+ years in leadership capacity.

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