ZipRecruiter

Log In

2

Remote Artiva Jobs (NOW HIRING)

All JobsArtiva JobsRemote Artiva Jobs

Remote Artiva information

See salary details

$69.5K

$129K

$183K

How much do remote artiva jobs pay per year?

As of Aug 14, 2026, the average yearly pay for remote artiva in the United States is $128,999.00, according to ZipRecruiter salary data. Most workers in this role earn between $108,000.00 and $144,500.00 per year, depending on experience, location, and employer.

What is a remote Artiva agent?

A Remote Artiva job typically involves working with the Artiva software platform, which is widely used in the collections and accounts receivable management industry. Employees in these roles may handle customer accounts, process payments, or manage debt collection activities, all while working remotely from home. The position often requires strong communication skills, experience with financial software, and the ability to work independently. Remote Artiva jobs are popular for their flexibility and the opportunity to work with clients from various industries. Training on the Artiva platform is usually provided by the employer.

What are some common challenges faced by a remote Artiva agent, and how can they be effectively managed?

Remote Artiva Agents, who typically work in collections or accounts receivable roles using Artiva software, often face challenges such as managing high call volumes, staying motivated while working independently, and maintaining compliance with regulations. To manage these challenges, it’s important to establish a structured daily routine, utilize Artiva’s automation tools to streamline workflows, and stay connected with team members through regular check-ins. Additionally, participating in ongoing training can help agents stay updated on best practices and compliance requirements.

What are the key skills and qualifications needed to thrive as a remote Artiva agent?

To thrive as a Remote Collections Agent working with systems like Artiva, you need strong communication skills, negotiation ability, and experience in accounts receivable or collections, often supported by a high school diploma or higher. Familiarity with Artiva collection software, CRM systems, and standard office applications is typically required. Empathy, resilience, and professionalism help you build rapport, handle difficult conversations, and maintain compliance. These skills are crucial for achieving collection targets, preserving customer relationships, and ensuring adherence to legal and organizational standards.

What is the difference between Remote Artiva vs Remote Data Analyst?

AspectRemote ArtivaRemote Data Analyst
Required CredentialsTypically requires a background in art, design, or creative fields; portfolio often neededRequires a degree in statistics, mathematics, or related fields; proficiency in data tools
Work EnvironmentCreative, collaborative teams often in marketing or media companiesAnalytical, often in tech, finance, or consulting firms
Industry UsageUsed mainly in creative industries, marketing, and advertisingCommon in finance, tech, healthcare, and consulting sectors

Remote Artiva roles focus on creative and artistic skills, often in marketing or media, while Remote Data Analysts handle data interpretation and analysis in various industries. Both roles are remote-friendly but require different skill sets and industry experience.

More about Remote Artiva jobs

What cities are hiring for Remote Artiva jobs?

Cities with the most Remote Artiva job openings:

What are the most commonly searched types of Artiva jobs?

The most popular types of Artiva jobs are:

What states have the most Remote Artiva jobs?

States with the most job openings for Remote Artiva jobs include:

What job categories do people searching Remote Artiva jobs look for?

The top searched job categories for Remote Artiva jobs are:

Remote Artiva jobs near you
Infographic showing various Remote Artiva job openings in the United States as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $128,999 per year, or $62 per hour.

Director / Senior Director of Regulatory Operations

Artiva Biotherapeutics

San Diego, CA • On-site, Remote

$268K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago

Job description

About Artiva: 

We are a clinical-stage biotechnology company focused on developing natural killer (NK) cell-based therapies. Our mission is to develop effective, safe, and accessible cell therapies for patients with devastating autoimmune diseases. We aim to develop therapies that patients and physicians can utilize in a community setting. Our lead product candidate, AlloNK®, is a non-genetically modified, cryopreserved NK cell therapy being evaluated in combination with B-cell targeted monoclonal antibodies (mAbs). We believe the compelling cell killing properties of NK cells, when combined with mAbs for targeting, creates an opportunity to generate potentially transformative therapies.


For more information, visit
www.artivabio.com.


Job Summary:

The Director / Senior Director of Regulatory Operations is responsible for building, leading, and scaling the regulatory operations function across Artiva’s growing portfolio of NK cell-based therapies. This role owns end-to-end submission planning, execution, and delivery for all global regulatory applications and will serve as the enterprise owner of our regulatory information management platform. The ideal candidate will bring deep expertise in eCTD submissions, regulatory information management systems, and cross-functional project leadership in a fast-paced biotech environment, with preference for experience in cell therapy or biologics. This role can be on-site or remote.


Duties/Responsibilities:

  • Build, lead, and scale Regulatory Operations at Artiva, establishing processes, infrastructure, and best practices to support Artiva’s expanding clinical and commercial portfolio.
  • Own end-to-end project planning and management, and on-time delivery of all regulatory submissions (INDs, CTAs, BLAs, MAAs, amendments, supplements, and annual reports) across global markets.
  • Serve as the regulatory information management system owner.
  • Partner with Regulatory Affairs Leads, Clinical Development, CMC, Pharmacovigilance, Project Management and Program Lead to develop and maintain integrated regulatory project plans, timelines, and risk mitigation strategies.
  • Lead cross-functional submission teams composed of internal stakeholders and external consultants; drive alignment, accountability, and execution to ensure zero-defect filings.
  • Develop and maintain real-time tracking dashboards and KPI reporting; proactively escalate risks and present submission status to senior leadership.
  • Author and maintain SOPs, work instructions, and templates governing the regulatory submission lifecycle, document management, and publishing/QC processes.
  • Ensure compliance with global regulatory requirements for electronic submissions, including eCTD formatting, validation, and publishing standards across US, EU, Canada, and other markets.
  • Provide strategic input on regulatory pathways, including Accelerated Approval, Breakthrough Therapy, Orphan Drug, and other expedited programs relevant to Artiva’s pipeline.
  • Manage and develop direct reports; recruit, mentor, and build a high-performing regulatory operations team.


Professional Experience/Qualifications:

  • Bachelor’s degree required; advanced degree preferred.
  • 15+ years’ experience in Regulatory Affairs, Regulatory Operations, and/or Regulatory Project Management within the biopharmaceutical or biotechnology industry, with at least 5 years in a leadership role.
  • Proven track record of leading end-to-end regulatory submissions (INDs, NDAs/BLAs, MAAs) with zero filing deficiencies, refuse-to-file actions, or delays.
  • Deep expertise with Veeva Vault RIM (Submissions, Archive, and/or Registrations modules) or similar platform, including hands-on implementation and administration experience.
  • Strong knowledge of eCTD structure, publishing, and validation requirements across US (FDA), EU (EMA), and other global markets.
  • Demonstrated success building and managing regulatory operations teams in fast-paced, growth-stage biotech or pharmaceutical companies.
  • Experience supporting programs utilizing FDA Accelerated Approval, Breakthrough Therapy Designation, Orphan Drug Designation, or other expedited regulatory pathways.
  • Hands-on experience in the preparation and submission of regulatory filings (e.g., INDs, CTAs, BLAs, and MAAs).
  • Excellent written and verbal communication and collaboration skills to work effectively with cross-functional teams.
  • Ability to thrive in a fast-paced environment and adapt to changing regulatory requirements.


In addition to a great culture, we offer:

  • A beautiful facility 
  • An entrepreneurial, highly collaborative, and innovative environment
  • Comprehensive benefits, including:
  • Medical, Dental, and Vision
  • Group Life Insurance
  • Long Term Disability (LTD)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Flexible Spending Account (FSA)
  • Paid Time Off (PTO)
  • Company paid holidays, including the year-end holiday week
  • Our recognition program, Bonus.ly, is where you can trade in points earned for things you want.


If all this speaks to you, come join us on our journey!


Base Salary: $205,000 - 268,000. Exact compensation may vary based on level, skills and experience.


Apply