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Study Director

Company: Amplifybio, LLC
Location: West Jefferson
Posted on: June 25, 2022

Job Description:

Do you want to be part of a growing world-class organization focused on bettering our world? Are you passionate about significantly improving the future of medicine? Do you believe that people are the most important asset of any company? If so, join AmplifyBio! AmplifyBio is a newly established, commercially focused preclinical CRO that was created as a Battelle spin-off. Aligned with, and supported by leading life sciences-focused investors, we partner with our clients to provide preclinical CRO services from single study and through full IND enabling studies. We have a strong focus and commitment to helping accelerate the commercialization of advanced therapies such as cell and gene therapies and vaccines. Moving forward we will combine continuous improvement and innovation to become the preferred preclinical CRO in the industry, by working in partnership with our clients, and leveraging state of the art technologies and platforms we will enable our customers to accelerate and improve the product development cycle, from concept to commercial.When you join our team, you will be a part of groundbreaking work while collaborating with our clients, research scientists, study directors, lab technicians and specialists across a variety of disciplines. Our chemists, biologists, veterinarians, data scientists, engineers, pathologists, and other experts collaborate to deliver new and exciting breakthroughs. The future for AmplifyBio is as great as the combination of our imaginations and actions, and we hold ourselves accountable for our choices and results. We have a bias for action, excellence, and, especially, the health and safety of our employees.AmplifyBio is seeking to hire a Study Director to join our growing team!!! The Study Director has oversight of the scientific elements of projects to ensure successful implementation and/or study completion of non-clinical studies. The individual filling this position must be knowledgeable of emerging trends and may contribute to and influence best practices within the discipline. This individual will analyze, and report results to our clients, provide scientific instruction to other members of the project team, and collaborate with other senior members of the staff on projects research. The individual is responsible for the organization, management, and business performance of the projects they will assigned. The Study Director will report to the Director of Study Oversight. What You'll Do Here: Serves as Study Director on toxicology, biodistribution, pharmacokinetic, and related studies to ensure study execution, client engagement, and deliverables upon study completion.Provides nonclinical expertise to a cross-functional project team. Partners with business development and project management to generate proposals and costings for new work.Works with internal functional areas to ensure all studies are performed in a quality, timely, and scientific manner. Drafts protocols, amendments, departmental notifications, and study comments forms, ensuring correct grammar, punctuation, consistency in format and style, and adherence to regulatory requirements and contract language.Follows GLP and other appropriate regulatory (e.g., OECD, ICH) requirements to ensure all experimental data, are accurately recorded and verified.Authors, updates, and/or reviews area-specific SOP's, ensuring that SOP's reflect current practices.Manages studies within time and budget constraints.Participates in continual improvement initiatives. We Would Love to Hear from You If: Bachelor's degree in life sciences related field with 5 years of experience or master's degree in related field with 2 years of experience or PhD; or an equivalent combination of education and or experience in a related field.Work within a GLP or similarly regulated environment.Excellent communication skills, with attention to detail, with the proven ability to build open and collaborative relationships and work effectively as a member of a multidisciplinary team.Excellent time management and organizational skills. Proven ability to handle multiple and changing priorities.Experience in the preparation and review of regulatory documents including writing the nonclinical safety assessment portion of regulatory documents.Experience creating and presenting scientific presentation and publications.Able and willing to work in a biosafety level 2 (BSL2) environment and wear appropriate PPE.Role will require immunization with FDA licensed vaccines and Investigational New Drugs (IND) recommended for persons at risk to occupational exposure of biological agents. At AmplifyBio, we're committed to growing and empowering an inclusive community within our company and industry. This is why we hire and cultivate diverse teams of the best and brightest from all backgrounds, experiences, and perspectives across our organization. Research shows that oftentimes women and minority groups only apply to open roles if they meet 100% of the listed criteria. AmplifyBio encourages everyone - including women, people of color, individuals with disabilities and those in the LGBTQIA+ community - to apply for our available positions, even if they don't necessarily check every box on the job description. Hire for attitude and train for aptitude creates unique opportunities to build strong teams of smart, motivated individuals who love what they do. AmplifyBio is an equal opportunity employer, and we value diversity at our company. We don't discriminate on the basis of race, color, citizenship status, national origin, ancestry, gender (including gender expression and gender identity), sexual orientation, age, weight, religion, creed, physical or mental disability, marital status, veteran status, political affiliation, or any other factor protected by federal, state, or local law. AmplifyBio will not tolerate discrimination or harassment based on any of these characteristics. If you have a disability or special need that requires accommodation, please let us know during the recruiting process. We are committed to the safety and wellness of our employees and customers. Therefore, COVID vaccination is required. Reasonable accommodations will be considered.Why You Will Love Working Here:We take the health and happiness of our employees seriously and consistently evaluate new ways to Amp up our benefits to provide an amazing place to work. From a wellness program (did we mention we have an onsite gym and ping pong table?), to financial planning and legal assistance, we make sure to take care of our own.Health, Dental, and Vision insurance that starts on your first day at AmplifyBioCompetitive Compensation Package We take work-life balance seriously and we back it up with generous PTOLife and AD&D insurance Supplemental insuranceLiveHealth OnlineSmart Shopper (helps you shop for better medical care and earn cash rewards while you save)4 weeks paid Parental LeaveWellness Program401(k) matchTuition Reimbursement EAP/work-life support systemA fun work environment where everyone's voice mattersWe are just getting started! More benefits on the way!An Opportunity to Change the World PI181787509

Keywords: Amplifybio, LLC, Columbus , Study Director, Executive , West Jefferson, Ohio

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