Qualifications include a Doctor of Veterinary Medicine degree, preferred board-certification, MBA or extensive business and leadership training, minimum of 7 years as a leader in an animal welfare/health organization, experience in marketing and corporate relations , solid knowledge of the animal welfare/health industry, ability to develop business strategies in line with the organization’s goals, must bridge diverse areas of expertise: medicine/surgery, toxicology, behavior, research, business strategy and marketing. Leadership and staff development skills are key, experience working with unions is helpful.

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Qualifications include a DVM with 3-5 years of veterinary practice experience. A PhD is a plus as well as someone who is a trail-blazer and champion of identifying new technologies and technology improvements.  Will need to have mastery at handling complex tasks & projects as well as multiple projects concurrently and will apply knowledge of technical and medical fields within category teams and peers.  The incumbent will aggressively seek new technology and IP protection and will stay abreast of new developments and opportunities.  Will need to represent the company via the media, web, conferences and veterinary outreach and will need to be an excellent technical writer and have a track record of publishing in peer reviewed scientific journals.  Will need the abiilty to design protocols for clinical trials whereby the outcome will support product claims.

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The Research Coordinator will communicate with and travel to designated study sites to conduct pre-study site evaluations, study initiation, interim monitoring and study close out visits for preclinical and clinical studies. The incumbent will establish rapport with subcontractors and study site personnel to facilitate communication and compliance with all study activities. Reviews the study records, casebooks and Investigator’s notebooks to ensure contents are current and complete including verification of owner consent, existence and maintenance of source documents and inventory of test supplies. Facilitates clarifications, corrections and data query resolution with study sites or data management, subcontractors and assists with responses to quality assurance audits. The incumbent will assist in management of study test article inventories and other related study materials. Depending on qualifications, may assist in the appropriate response to, and documentation of, adverse events. May serve as Project Manager and have oversight of all communications with a client for a specific clinical study. As Project Manager will coordinate the allocation of monitoring and quality control resources to best meet client needs, including scheduling and oversight of Clinical Research Coordinators. Serves as an ambassador for the company to generate new business and new business leads.

Qualifications include DVM or VMD. Good communication skills, good active listening skills. Experienced in GCP trials, 3-5 years of practice experience. Excellent interpersonal skills. Ability to travel 75% of the time. Basic computer skills, valid driver’s license with clean driving record, willingness to travel. Minimum Experience in data management, quality control and/or quality assurance is helpful.

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Incumbent will work closely with department heads and develop and share metrics across the organization to build financial understanding and achieve aggressive growth plans. CFO will build a lean finance team as the company grows.

Incumbent will ensure strong financial controls, including managing audits, while supporting an entrepreneurial and performance driven culture.

CFO will be energetic, stellar communicator as well as an open and supportive team builder.  CFO will enjoy learning the business, from our manufacturing partners to our key customers and will be passionate about building a company and its infrastructure to listen to customers: companion animal veterinarians.

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Qualifications include a BS/MS/PhD in science or related field with 10+ years relevant work experience in Regulatory Affairs. Pet Care Regulatory Affairs experience is a plus. In depth knowledge of AFFCO and or EPA regulations. FDA experience is a plus.

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The Director must be able to proactively address and lead resolution of compliance issues internally and with external partners and contractors and must have at least 8 years experience in Quality Assurance for a human or animal drug company and will have substantial knowledge of cGMP requirements for multiple dosage forms, along with prior experience with supplier qualification. Additional experience with GDPs and/or GLPs is desirable. International and domestic travel required.

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The incumbent will review and ensure accuracy of various reports and documents for FDA submissions; manage and maintain regulatory and product development document systems;  track and maintain current state manufacturing and distributor licenses;  manage administrative tasks for bioequivalence studies; maintain product development project timelines and meeting minutes.

Must have at least 2 years experience in a pharmaceutical QA role.

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The Research Coordinator will communicate with and travel to designated study sites to conduct pre-study site evaluations, study initiation, interim monitoring and study close out visits for preclinical and clinical studies. The incumbent will establish rapport with subcontractors and study site personnel to facilitate communication and compliance with all study activities. Reviews the study records, casebooks and Investigator’s notebooks to ensure contents are current and complete including verification of owner consent, existence and maintenance of source documents and inventory of test supplies. Facilitates clarifications, corrections and data query resolution with study sites or data management, subcontractors and assists with responses to quality assurance audits. The incumbent will assist in management of study test article inventories and other related study materials. Depending on qualifications, may assist in the appropriate response to, and documentation of, adverse events. May serve as Project Manager and have oversight of all communications with a client for a specific clinical study. As Project Manager will coordinate the allocation of monitoring and quality control resources to best meet client needs, including scheduling and oversight of Clinical Research Coordinators. Serves as an ambassador for the company to generate new business and new business leads.

Qualifications include Bachelor’s degree, preferably in a scientific discipline or significant experience in a similar role. An advanced degree (MS, DVM or VMD) is highly desirable. Good communication skills, good active listening skills. Basic computer skills, valid driver’s license with clean driving record, willingness to travel.  Minimum of six years including experience participating and/or managing animal health clinical studies for Senior Research Coordinator role. Experience in data management, quality control and/or quality assurance is helpful.

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