Gene Therapy Experts – Full Time & Per Diem

Pharmavise Corporation; United States; Remote; USD 120,000 - 180,000; Full time

Benefits offered by this job

Flexible scheduling

Per diem roles

Job summary

PharmaviseConsulting Corp. seeks experienced professionals to lead gene therapy research and development projects from discovery to clinical development. You will design experiments, optimize vectors, and collaborate across research, preclinical, clinical, and regulatory teams to advance programs.

The role requires a PhD or equivalent and at least 5 years in gene therapy, with strong knowledge of regulatory guidelines and viral vector platforms. Remote work options are available.

Qualifications

• PhD or equivalent degree in molecular biology, genetics, biotechnology, or related field.
• Minimum 5 years of gene therapy R&D experience in biotech/pharma.
• Strong vector design, optimization, and characterization skills.
• Experience with gene editing (CRISPR/Cas9) and viral vectors (AAV, lentivirus).
• Knowledge of FDA/EMA regulatory guidelines for gene therapy development.
• Excellent analytical and problem-solving abilities; strong collaboration.
• Leadership experience is preferred but not required.

Responsibilities

• Lead and contribute to gene therapy R&D projects from discovery to clinical development.
• Design experiments to optimize vectors, transgene expression, and delivery.
• Develop strategies for manufacturing scalability and vector design challenges.
• Collaborate with research, preclinical, clinical, and regulatory teams.
• Stay updated on regulatory requirements and scientific advancements.
• Contribute to regulatory submissions (INDs, BLAs, orphan drug applications).
• Mentor junior staff and collaborators on gene therapy projects.

Skills

Gene therapy

CRISPR/Cas9

Viral vectors

Analytical thinking

Leadership experience

Education

PhD or equivalent degree

Tools

CRISPR/Cas9

AAV

Lentivirus

Job description

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.

We are actively seeking skilled and knowledgeable professionals to join our team.

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 platforms (e.g., AAV, lentivirus).
• Knowledge of regulatory requirements and guidelines governing gene therapy product development (e.g., FDA, EMA).
• Excellent analytical and problem-solving skills, with the ability to design and interpret complex experiments.
• Effective communication and collaboration skills, with the ability to work in a fast-paced, team-oriented environment.
• Leadership experience and a track record of successfully leading gene therapy projects preferred but not required.

Benefits

• We offer competitive compensation packages, including comprehensive benefits for full-time positions, and flexible scheduling options for per diem roles.

EEO Employer: PharmaviseConsulting Corp. is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. PharmaviseConsulting Corp. will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law.

PharmaviseConsulting Corp. is a regulatory compliance consulting firm that partners with Pharmaceutical, Medical Device and Biotechnology clients.

When you joinPharmavise, you become part of a team that values Excellence Through Quality.

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