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Nutramax Laboratories, Inc. seeks an Associate Director of Clinical Affairs to oversee downstream clinical activity, PSV/FSV and KOL management. You will drive scientific messaging, develop training materials, publications, and events, and advise on product development and launch strategy through field teams.
A minimum of five years in the veterinary industry is expected. You will lead CE programs and VOC initiatives, collaborate with R&D and Commercial to differentiate products, and support
All Jobs > Associate Director of Clinical Affairs
Nutramax desires to provide a drug-free, healthful, and safe workplace. We hold a zero-tolerance policy for drug use. Employment is contingent upon successfully passing a preemployment background check and drug screen (subject to applicable law).
The standard hours for this position are Monday - Friday 8:30am - 5:00pm.
This role is 100% on site at our Headquarters location: 946 Quality Drive, Lancaster, SC 29720.
The Associate Director of Clinical Affairs will be responsible for all downstream clinical activity and technical collateral. This will include oversight of Professional Service Veterinarians (PSV), Field Service Veterinarians (FSV), and key opinion leader (KOL) management. In this role you will spearhead communication between Nutramax, veterinary professionals, and pet parents. You will support the commercial organization in communicating scientific and clinical information through channels including training materials, product collateral, veterinary publications, and events. You will additionally advise the organization on product development and launch strategy driving execution through FSVs and KOLs. Success in this role will be measured based upon execution of strategic objectives, growth of focused products, and completion of targeted field activities. A successful candidate will have a minimum of five years of industry experience, ideally working for a manufacturer of nutraceutical or pharmaceutical products.