AAVantgarde Bio is a clinical stage, Italian headquartered, international biotechnology company that has developed two proprietary Adeno-Associated Viral (AAV) vector platforms to address the gene therapy cargo capacity limitations of AAV vectors. This platform is being clinically validated in two Inherited Retinal Diseases; Usher1B and Stargardt disease, and the platform is expected to address the gene therapy cargo capacity limitations of AAV vectors and therefore the future pipeline could extend into many disease areas.
AAVantgarde BIO is working to start a first-in-man proof of concept (POC) study in subjects with Usher1B and further develop and implement AAV intein program and entry into the clinic for Stargardt disease.
What you bring:
- PhD in Biology/Molecular Biology or related scientific area.
- Proven experience in the field of gene or cell therapy.
- Experience with animal models of ocular diseases and with AAV biology defines the ideal candidate.
- Experience in translational research, IND-enabling study planning and regulatory aspects, is a plus.
- Positive attitude, ability to work in teams, excellent verbal, written, and interpersonal communication skills. Strong ability in managing scientific programs high levels of accuracy in data recording and analysis, problem solving skills.
- Computing skills, including word processing and use of spreadsheets (e.g. Word, Excel, PowerPoint, etc.)
- Spoken and written English
In this role:
- you will have the opportunity to contribute to the development of the current programs for human ocular diseases, by executing scientific and technical activities and by also designing, authoring, and reviewing protocols, reports and regulatory documentations to support development/translational activities performed by the AAVantgarde BIO team directly or through CDMOs/CROs.
- you will support the development of a novel research pipeline and/or platform implementation and will use your expertise to translate discovery to therapeutics.
- you will provide support and interaction with the internal regulatory and clinical teams
What we offer:
- The opportunity to work in and advance cutting-edge science, and be part of a new generation of gene therapy medicines
- The chance to work with, and learn from, leaders in their fields
- The ability to advance your career and learning
- Competitive salary and benefits
To apply for the position please send your CV together with a cover letter to [email protected]
