Associate Director, Strategic Alliance (Genetic Medicine)

Benefits

Parental leave

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Non-birth-parent leave

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Family-building benefits

• Fertility benefits: Not verified
• Adoption assistance: Not verified
• Surrogacy assistance: Not verified

Mental health support

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Relocation assistance

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Childcare support

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Learning budget

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Verification

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Salary

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Market context

U.S. role benchmark (BLS OEWS)

$57,704 U.S. median for this role

Projected growth (BLS Employment Projections)

+0.9% - Slower

Matched to SOC 41-2031 - Sales aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function

Sales From the posting source checked Jun 20, 2026

Seniority

Director Plus From the posting source checked Jun 20, 2026

Work mode

Remote From the posting source checked Jun 20, 2026

In-office days

0 days From the posting source checked Jun 20, 2026

Schedule

Shift type

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Weekend work

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Application

Cover letter

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Assessment

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Deadline

Not stated

Where they hire

State eligibility is not yet verified.

About this role

Associate Director, Strategic Alliance (Genetic Medicine) Remote Our mission at Asimov is to advance humanity's ability to design living systems, enabling biotechnologies with outsized societal benefits. We're developing a mammalian synthetic biology platform--from cells to software--to enable the design and manufacture of next-generation therapeutics. The Associate Director, Strategic Alliance (Genetic Medicine) will play a pivotal role in supporting the deployment of our AAV Edge, RNA Edge, and LV Edge technologies in customer sites and delivering on cell line development (CLD) service campaigns for our customers. Asimov's LV Edge and AAV Edge technologies represent a fundamental shift in genetic medicines, moving the industry beyond the limitations of transient transfection by combining genetic design with high-performance, stable producer cell lines, to achieve higher, more consistent viral titers. This role involves building and nurturing long-term, mutually beneficial relationships with pharmaceutical and biotech companies, technology providers, academic institutions, and other strategic partners. About the Role: Program Execution - Provide expert technical guidance on tech-out evaluation design, CLD planning, scale-up, optimization, and troubleshooting for various biopharmaceutical manufacturing processes (e.g., mammalian cell culture, purification, analytical methods, and viral vector production). - Work cross-functionally with internal departments (CLD, DNA Assembly, Process Development, Analytical Development, Quality, Facilities, Business Development) to ensure project success. - Oversee the preparation and review of critical documentation, including tech transfer plans, protocols, CLD reports, cell history documentation, and drug master filings. - Develop and implement standardized tech transfer procedures, protocols, and

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