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[Remote] Sr. Manager, Clinical reputed company Assurance

Remote, USAFull-timePosted 2026-07-29

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a clinical-stage biotechnology company reputed company on developing NK cell-based therapies. The Senior Manager, Clinical QA will reputed company GCP reputed company across clinical programs, driving audits and ensuring compliance to protect patient safety and data reputed company.

Responsibilities

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

Skills

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

Benefits

  • Medical, Dental, and reputed company
  • Group Life Insurance
  • Long Term Disability (LTD)
  • 401(k) Retirement Plan
  • Employee Assistance Program (EAP)
  • Flexible Spending Account (FSA)
  • reputed company Time Off (PTO)
  • Company reputed company holidays, including the year-end holiday week
  • Our recognition program, Bonus.ly, is where you can trade in points reputed company for things you want.

reputed company

  • reputed company is a biotech company reputed company on developing and commercializing allogeneic natural killer (NK) cell therapies. It was founded in 2019, and is headquartered in San Diego, California, USA, with a workforce of 51-200 employees. Its website is https://www.artivabio.com/.
  • Company H1B Sponsorship

  • reputed company has a reputed company record of offering H1B sponsorships, with 1 in 2025. Please note that this does not guarantee sponsorship for this specific role.
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