Artiva Jobs (NOW HIRING)

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:
This is an exciting opportunity to join Artiva as we continue expanding our impact in cell therapy. As Senior Manager, Clinical QA, you'll lead risk-based GCP oversight across our clinical programs — driving audits, investigations, and inspection readiness that protect patients and data integrity from first-in-human through approval. You'll represent Clinical QA on study teams, collaborating closely with all development functional areas to embed quality into every stage of the program.

Essential Duties & Responsibilities:
•    Serve as the Clinical QA lead for assigned clinical programs and provide quality oversight across all phases of clinical development to ensure compliance with ICH-GCP, applicable regulations, and Artiva’s procedures.
•    Implement and conduct risk-based GCP quality oversight strategies for assigned clinical programs.
•    Conduct investigations of clinical investigator site issues, GCP quality issue investigations, determine root cause, corrective and preventive actions, and ensure appropriate and adequate documentation.
•    Plan, conduct/manage contract auditors, and oversee risk-based routine and for-cause audits of investigator sites, CROs, vendors, processes. 
•    Assess and communicate the impact of audit findings on PI/Sponsor oversight, subject safety, data integrity, and business operations.
•    Maintain required documentation and quality records in accordance with Artiva procedures. 
•    Support inspection readiness activities and participate in regulatory health authority inspections and inspection response activities.
•    Interact with internal teams and supporting functions to ensure quality compliance across all aspects of clinical development.
•    Represent Clinical QA on study teams and work collaboratively with all development functional areas.
•    Review key company documents associated with INDs, protocols, Investigator Brochure(s) and other relevant clinical trial documents for compliance with applicable regulations.
•    Implement a strategy to provide a review of key regulatory documents associated with regulatory submissions.
•    Identify GCP compliance risks and develop appropriate courses of action in partnership with the Clinical Department.
•    Maintain awareness of emerging regulations, guidance documents, and best industry practices and communicate relevant changes to management.
•    Provide QA consultation and participate in risk-based sponsor oversight activities.
•    Support and deliver GCP training for Clinical Operations staff, contributing to the broader clinical quality training program.
•    Present quality metrics and trend analyses.

Education and Experience:

• BS or BA in a scientific field.
• 6+ years of clinical and/or QA experience in biologics or pharma.
• 3+ years of Clinical QA experience.
• Knowledge and hands on experience in regulatory inspections, clinical investigator site/vendor/internal audits
• Thorough knowledge of current Good Clinical Practices as they relate to all phases of cell therapy product human clinical trials.
• Expert level of understanding of CLIA, CLIP, CAP.
• Knowledge of ICH, GCP, GCLP, Data Privacy and other applicable regulations and requirements in the pharmaceutical/biopharma industry.
• Sound basis of scientific (Training/Communications) knowledge.
• Expert knowledge of quality regulations, current industry practices, and strong experience with interpretation and application.
• Computer skills required to operate Microsoft Word, Project, and Excel programs.

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: $ 150,000 - $172,000. Exact compensation may vary based on level, skills and experience.