Job Summary: A Study Director will serve as a Principal Investigator working with clients in defining the objectives, strategies and project design for internal and external in-vivo studies. They will also ensure that all the research is done correctly and promptly to ensure objectives are met. The Study Director will oversee data reporting, data QC and release of data to clients for interpretation, responsible for the development of applicable protocols/plans in accordance with study-specific procedures, company standard operating procedures (SOPs), industry regulatory guidelines, and budgetary guidelines to meet business/scientific needs. The Study Director will be responsible for growing and providing scientific oversight of our pre-clinical in vivo service portfolio. The individual in this role will play a role in developing new procedures in support of ocular model development, collecting and analyzing study endpoints, procuring the necessary equipment and materials for model development, mentoring and training Associate Scientists and staff. Essential Functions: Fulfill the role of Study Director on in-vivo studies.The individual in this position is expected to possess the ability to manage projects and studies, delivering projects on time and within budget. The ability to problem solve, communicate effectively with staff and clients are part of this position.Train and mentor junior staff on the necessary procedures and equipment.Ability to design, execute and interpret experiments and studies.Conducts research, analyzes results and provides technical direction to others in research and results analysis.Evaluates possible research projects and participates in the planning of new projects.Adherence to regulations, study protocols, PharmOptima’s SOPs, policies and best practices. Knowledge and use of good documentation and laboratory practices. Researches and reviews applicable federal guidelines and protocols; changes procedures to ensure compliance.Responsible for writing appropriate new SOPs and updating current SOPs to follow best practices.Extensive hands-on experience in the conduct of in vivo studies in multiple species.Perform the necessary model development, validation, and implementation of ocular efficacy models.Other duties as assigned or pertaining to experience and licensure. Education and Experience:Experience: 5 years related experience working with animals in a pre-clinical laboratory or clinical setting; experience working in a CRO with multi-species preferred.MS/Ph.D. preferred.Must have demonstrated expertise with a variety of animal species with a focus on rodents and rabbits. Experience working in a regulatory controlled environment, adhering to SOPs preferred.Experience in a GLP environment preferred.Excellent organizational skills, especially with time management and record keeping. Demonstrated analytical and problem-solving skills. Ability to lead independently. Must be proficient in the use of computers. Must be able to work independently. Excellent communication skills both written and verbal.