Implementation Specialist

Benefits

Parental leave

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Non-birth-parent leave

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Family-building benefits

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• 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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401(k) match

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Market context

U.S. role benchmark (BLS OEWS)

$116,543 U.S. median for this role

Projected growth (BLS Employment Projections)

+9.8% - Much faster than average

Matched to SOC 15-1252 - Software Engineering aggregate by role bucket.

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

Role

Role function

Engineering From the posting source checked Jun 20, 2026

Seniority

Mid From the posting source checked Jun 20, 2026

Work mode

Hybrid From the posting source checked Jun 20, 2026

In-office days

2 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

Implementation Specialist San Francisco | Hybrid | Remote ABOUT ARTOS: At Artos, we build tools that help biopharma companies create and manage their R&D documentation in a fraction of the time. If you're looking to join a team whose mission is to fundamentally change the way that drug development gets done, we'd love to talk to you. We're growing very fast, and we're looking for a domain-expert technical product lead-someone with a strong pharma background who can sit between engineering teams and end users, help implement our system in real customer environments, and translate deeply technical capabilities into workflows that actually make sense to scientists, medical writers, and regulatory teams. This is not a traditional product manager role, and it is not a traditional medical writing role. It's a hybrid: part domain architect, part technical translator, part customer-facing problem solver. The Role: As a core member of Artos's product team, you will act as the bridge between engineering and domain experts. Your primary responsibility will be to help design, implement, and evolve systems that generate and manage regulatory and R&D documentation-particularly in the non-clinical and/or CMC domains-by ensuring that domain reality is faithfully represented in the pro duct. You will work closely with: - End users: (medical writers, regulatory professionals, scientists) to understand how documents are actually authored, reviewed, and quality-controlled in practice - Engineering teams: to translate those workflows, constraints, and edge cases into system behavior - Product leadership: to shape feature scope, prioritization, and release readiness You will

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