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Jobs at Artiva Biotherapeutics (Now Hiring) — 11 open

Artiva Biotherapeutics logoArtiva Biotherapeutics

Sr. Director/ED, Medical Affairs Medical Communications Publications

San Diego, California, United States · Remote OK

$250k–$300k/yr

Senior+$198M raised

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 devas…

Skills: Publication Planning, Medical Communications, Scientific Storytelling, Agency Management, Congress Strategy

Artiva Biotherapeutics logoArtiva Biotherapeutics

Validation Engineer II

San Diego, California, United States · On-site

$87k–$103k/yr

Mid level$198M raised

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 devas…

Skills: GMP Validation, Technical Writing, Risk Assessment, FMEA, IQ/OQ/PQ Execution

Artiva Biotherapeutics logoArtiva Biotherapeutics

Calibration Technician II

San Diego, California, United States · On-site

$70k–$85k/yr

Mid level$198M raised

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 devas…

Skills: Calibration, GMP Compliance, Preventive Maintenance, Troubleshooting, CMMS/QMS

Artiva Biotherapeutics logoArtiva Biotherapeutics

Senior Manager / Associate Director, CMC Project Management - Process Development & Validation

San Diego, California, United States · Hybrid

$155k–$190k/yr

Senior$198M raised

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 devas…

Skills: CMC Project Management, Process Characterization, Process Performance Qualification, GMP Manufacturing, CDMO Management

Artiva Biotherapeutics logoArtiva Biotherapeutics

People and Culture Coordinator

San Diego, California, United States · On-site

$75k–$90k/yr

Mid level$198M raised

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 devas…

Skills: HR Operations, Onboarding, Offboarding, Recruiting Coordination, HR Systems Administration

Artiva Biotherapeutics logoArtiva Biotherapeutics

Supervisor, Quality Control Biology

San Diego, California, United States · On-site

$110k–$135k/yr

Senior+$198M raised

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 devas…

Skills: cGMP, Quality Control, ELISA, Flow Cytometry, SOP Writing

Artiva Biotherapeutics logoArtiva Biotherapeutics

Associate II, Quality Control Biology

San Diego, California, United States · On-site

$79k–$91k/yr

Mid level$198M raised

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 devas…

Skills: cGMP, ELISA, Flow Cytometry, Analytical Validation, Technical Writing

Artiva Biotherapeutics logoArtiva Biotherapeutics

Associate II/III, Quality Control Environmental Monitoring

San Diego, California, United States · On-site

$77k–$93k/yr

Senior$198M raised

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 devas…

Skills: Environmental Monitoring, Aseptic Techniques, cGMP Compliance, Root Cause Analysis, CAPA

Artiva Biotherapeutics logoArtiva Biotherapeutics

Director, Biostatistics

San Diego, California, United States · Hybrid

$215k–$250k/yr

Senior+$198M raised

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 devas…

Skills: Biostatistics, Clinical Trial Design, Statistical Analysis Plan, SAS, R

Artiva Biotherapeutics logoArtiva Biotherapeutics

Scientist I/II, Pharmacology and Translational Science

San Diego, California, United States · On-site

$120k–$142k/yr

Mid level$198M raised

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 devas…

Skills: Flow Cytometry, ELISA, MSD Platform, ddPCR, qPCR

Artiva Biotherapeutics logoArtiva Biotherapeutics

Director, Corporate Development & Strategy

San Diego, California, United States · Hybrid

$200k–$230k/yr

Senior+$198M raised

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 devas…

Skills: Corporate Strategy, Commercial Planning, Business Development, Financial Modeling, Competitive Intelligence

Artiva Biotherapeutics logo

Sr. Director/ED, Medical Affairs Medical Communications Publications

Artiva Biotherapeutics

San Diego, California, United States • Remote OK

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  • $250k–$300k/yr
  • Full-time
  • postgraduate degree
  • Medical Insurance, Dental Insurance, Vision Insurance, Group Life Insurance, Long Term Disability (LTD), 401(k) Retirement Plan
  • Posted 5d ago
  • ~40 hrs/week
  • Remote in United States

Responsibilities

Drive the end-to-end strategic planning and execution of scientific publications and congress activities for the AlloNK platform. Translate complex clinical data in rheumatology and immunology into high-impact, compliant scientific communications.

Requirements

Requires an advanced scientific or clinical degree (PhD, PharmD, DO, or MD) and over 8 years of medical communications experience in biotech or pharma. Must have deep expertise in rheumatology, immunology, or cell therapies and expert knowledge of ICMJE and GPP guidelines.

Full 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 Sr. Director/Executive Director, Medical Communications Publications will drive the end-to-end strategic planning and execution of scientific publications across the AlloNK platform and lead comprehensive congress activities. Operating at the intersection of R&D and Medical Affairs, you will translate complex clinical data in rheumatology, cell therapy, and immunology into compelling, compliant, and high-impact scientific communications. We are looking for someone who is equally comfortable setting up the strategy and rolling up their sleeves — a hands-on leader who can build and inspire a team while delivering results.

Key Responsibilities

  • Publication Planning & Strategy: Develop and execute global/regional publication plans (abstracts, posters, manuscripts, reviews) for rheumatology, immunology, and cell therapy audiences.
  • Data Dissemination: Collaborate with Clinical Development, Medical Affairs, and principal investigators to ensure timely, accurate dissemination of clinical trial results at major scientific congresses.
  • Compliance & Governance: Ensure all publications strictly adhere to Good Publication Practice (GPP), ICMJE authorship guidelines, and corporate compliance standards.
  • Content Development & Review: Oversee the drafting, editing, and medical review of scientific publications and related congress materials, ensuring scientific accuracy and balanced data presentation.
  • Agency Management: Direct external medical communications agencies, medical writers, and vendor budgets to ensure on-time, high-quality deliverables.
  • Congress Planning & Strategy: Architect the comprehensive pre- and post-congress communication strategy for major rheumatology and immunology meetings (e.g., ACR, EULAR, ISSJD, CCR) including congress playbooks and post-congress debriefs.
  • Medical Affairs Activities: Lead the development of congress-specific materials, including scientific symposia, medical booth content, and interactive learning stations.
  • Competitive Intelligence: Monitor emerging clinical data, treatment paradigm shifts, and competitor activity at key meetings, translating these external insights into actionable communication strategies.


Qualifications

  • Advanced scientific or clinical degree (e.g., PhD, PharmD, DO, or MD) required.
  • 8+ years of progressive medical communications or publications experience within the biotech or pharmaceutical industry.
  • Proven track record and deep understanding of rheumatology, immunology, and/or complex cell therapies (e.g., CAR-T, TCEs).
  • Expert knowledge of ICMJE guidelines, GPP guidelines, and the Sunshine Act/EFPIA disclosure requirements.
  • Demonstrated ability to lead cross-functional teams, build a medical communications and publications capability, manage and mentor junior staff, and manage multiple complex projects simultaneously.

Preferred Skills

  • Experience utilizing publication management software (e.g., Datavision) to track publication progress and manage author review cycles.
  • Strong network of relationships with Key Opinion Leaders (KOLs) in rheumatology, immunology, and cell therapy.
  • Exceptional scientific storytelling ability and meticulous attention to detail.
  • ISMPP CMPP certification

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: $250,000 - 300,000. Exact compensation may vary based on level, skills, and experience.

Related keywords

AlloNKNK Cell TherapyRheumatologyImmunologyGPPICMJESunshine ActEFPIADatavisionISMPP CMPPClinical TrialsMedical AffairsScientific PublicationsCAR-TTCEsBiotechnology

About Artiva Biotherapeutics

LinkedInVisit site

We are dedicated to making safe and effective cell therapies accessible to any cancer patient who may benefit.

Industry
Biotechnology Research
Company size
51-200 employees
Founded
2019
Headquarters
San Diego, California
LinkedIn followers
14,399
Total funding
$198M

Artiva Biotherapeutics is an immunotherapy company with the ability to produce off-the-shelf, allogeneic NK cell therapies at a massive scale. Our mission is to develop effective, safe and accessible cell therapies for patients with devastating autoimmune diseases and cancers. Our lead program, AlloNK®, is an allogeneic, non-genetically modified NK cell therapy candidate designed to enhance the activity of monoclonal antibodies or NK cell engagers. AlloNK is currently in clinical trials in combination with rituximab for treatment of systemic lupus erythematosus (SLE) in patients with active lupus nephritis and for treatment of Non-Hodgkin Lymphoma, as well as in combination with Affimed’s innate cell engager AFM13 for the treatment of patients with relapsed/refractory CD30-positive lymphomas.

Offices: 5505 Morehouse Drive, Suite 100, San Diego, California 92121, US

cell therapycancernk cellsnk cell therapyand car-nkBiotechnologyLife ScienceTherapeutics
View all jobs at Artiva Biotherapeutics

About Artiva Biotherapeutics

LinkedInVisit site

We are dedicated to making safe and effective cell therapies accessible to any cancer patient who may benefit.

Industry
Biotechnology Research
Company size
51-200 employees
Founded
2019
Headquarters
San Diego, California
LinkedIn followers
14,399
Total funding
$198M

Artiva Biotherapeutics is an immunotherapy company with the ability to produce off-the-shelf, allogeneic NK cell therapies at a massive scale. Our mission is to develop effective, safe and accessible cell therapies for patients with devastating autoimmune diseases and cancers. Our lead program, AlloNK®, is an allogeneic, non-genetically modified NK cell therapy candidate designed to enhance the activity of monoclonal antibodies or NK cell engagers. AlloNK is currently in clinical trials in combination with rituximab for treatment of systemic lupus erythematosus (SLE) in patients with active lupus nephritis and for treatment of Non-Hodgkin Lymphoma, as well as in combination with Affimed’s innate cell engager AFM13 for the treatment of patients with relapsed/refractory CD30-positive lymphomas.

Offices: 5505 Morehouse Drive, Suite 100, San Diego, California 92121, US

cell therapycancernk cellsnk cell therapyand car-nkBiotechnologyLife ScienceTherapeutics
View all jobs at Artiva Biotherapeutics

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