Gene Therapy Experts – Full Time & Per Diem

This is a remote position. From development to commercialization, we partner with Pharmaceutical, Medical Device and Biotechnology clients to provide solutions to complex compliance issues. We collaborate with our partners by providing technical expertise in Quality, Regulatory Compliance and Manufacturing Science and Technology. Our business mission is to ensure our clients exceed their compliance goals while improving patient health and safety. Visit us at www.pharmavise.com We are actively seeking skilled and knowledgeable professionals to join our team asGene Therapy Experts – Full Time & Per Diem. Below, you'll find a comprehensive job description detailing the responsibilities, qualifications, and expectations for this role: Responsibilities: Lead and contribute to gene therapy research and development projects from early discovery through to clinical development. Design and execute experiments to optimize gene therapy vectors, transgene expression, and delivery systems. Develop and implement innovative strategies to address challenges related to gene therapy vector design, manufacturing, and scalability. Collaborate cross-functionally with research, preclinical, clinical, and regulatory teams to advance gene therapy programs. Stay abreast of emerging technologies, scientific advancements, and regulatory requirements in the field of gene therapy. Contribute to the preparation and review of regulatory submissions, including INDs, BLAs, and orphan drug applications. Mentor and provide guidance to junior staff members and collaborators working on gene therapy projects. Qualifications: PhD or equivalent degree in molecular biology, genetics, biotechnology, or related field. Minimum of 5 years of experience in gene therapy research and development within the biotechnology or pharmaceutical industry. Strong expertise in gene therapy vector design, optimization, and characterization. Experience with gene editing technologies (e.g., CRISPR/Cas9) and viral vector platf