Aaron Johnson Dvm, Ms Email & Phone Number

United States

United States

United States

Indianapolis Area

Work as a weekend relief veterinarian at several small animal veterinary hospitals in the Indianapolis area. Practice responsibilities include the diagnosis and treatment of medical conditions (including but not limited to dermatology, cardiac, renal, gastrointestinal, musculoskeletal, neurologic, endocrine/metabolic, behavioral, ophthalmic, and other internal conditions), advocating and delivering preventative care, and client education.

Greenfield, Indiana, United States

Create and lead project teams across cross-functional areas in a matrix organization (safety/toxicology, DMPK, efficacy & model development, technical development, project management, regulatory) to advance pet health therapeutic projects into development. Create project development plans with a focus on risk identification and mitigation, robust scientific strategy, timeline accountability, and budget management. Contribute to scientific strategy discussions, provide input into relevant study design and protocol discussions, contribute to data review, and ensure the team is aligned on study outcomes and conclusions. Ensure technical requirements are complete and in-line with internal processes, and represent the project and the project team at governance milestone reviews and decisions with senior management. Collaborate with research and development teams to ensure efficient progression and transition of projects into and out of Exploratory Development. Review literature for new therapeutic targets with translational potential for companion animals, develop strong working relationships with internal stakeholders to drive ideation in key companion animal therapeutic areas, establish and maintain relationships with key external partners and key opinion leaders, and contribute to evaluation of external opportunities.

Greenfield, Indiana

Create and lead project teams within a hybrid matrix organization to advance projects into development, while simultaneously serving as the efficacy and model development lead for those projects. Create project development plans with a focus on risk identification and mitigation, robust scientific strategy, timeline accountability, and budget management. Work closely with project managers to develop accurate timelines and budget forecasts to ensure project delivery in a high quality, timely, cost-effective manner. Represent the project and the project team at governance milestone reviews and decisions with senior management. Actively contribute to scientific strategy discussions, provide scientific input into relevant study designs and protocols, review study data, and ensure the team is aligned on study outcomes and conclusions. Identify, develop, and validate new laboratory models for companion animal therapeutic conditions. Design and conduct early (e.g., proof of principle and proof of concept) target animal efficacy studies. Develop and maintain relationships with contract research organizations (CROs), external partners, and key opinion leaders. Collaborate with development teams to efficiently progress and transition projects into development. Review literature for new therapeutic assets or targets with translational potential for companion animals, develop strong working relationships with internal stakeholders to drive ideation in key companion animal therapeutic areas, and contribute to evaluation of external opportunities.

Greenfield, Indiana

Provide regulatory, scientific, and technical expertise (effectiveness, safety/toxicology, pharmacokinetics) to the companion animal R&D project teams for both parasiticide and therapeutic products, in addition to select food animal projects. Provide cross-functional leadership to the development and execution of regulatory strategy across key internal stakeholders. Coordinate the preparation of investigational new animal drug (INAD) submissions, agency meeting requests, protocols, responses, general correspondences, major and minor technical section submissions (effectiveness, target animal safety, environmental, labeling, and all other information), and new animal drug applications with the FDA Center for Veterinary Medicine (CVM). Coordinate the preparation of pesticide registration applications, notifications and amendments, meeting requests, protocols, responses, and general correspondences with the U.S. Environmental Protection Agency (EPA). Lead meetings with the CVM and EPA to align upon project development plans, clinical and non-clinical study designs, study outcomes, and product label verbiage. Maintain training and working knowledge of Good Clinical Practice (GCP) and Good Laboratory Practice (GLP) standards. Support the approval and launch of Elanco products following regulatory approval. Evaluate new technologies and drug candidates as a regulatory due diligence representative. Supervise and support a sub-team of companion animal regulatory scientists.

Westfield, Indiana

Practice responsibilities include the diagnosis and treatment of medical disorders, performing a wide range of soft tissue surgical procedures, advocating preventative care, and client education. Primary facilitator of dental care, including dental radiography, treatment of periodontal disease, complex surgical extractions, and oral surgery.

Fishers, Indiana

Practice responsibilities include the diagnosis and treatment of medical disorders, performing a wide range of soft tissue surgical procedures, advocating preventative care, and client education. Special interests include dentistry, internal medicine, and diagnostic imaging.

Dvm, Veterinary Medicine

Activities and Societies: Omega Tau Sigma veterinary fraternity (President 2002-2004) Student Chapter of American Veterinary Medical.

Ms, Reproductive Physiology

Activities and Societies: Society for the Study of Reproduction International Embryo Transfer Society

Bs, Animal Science

Activities and Societies: Purdue Roller Hockey Club Purdue Pre-Vet Club