Full-Time

Director – Clinical Quality

Updated on 4/9/2024

Arcellx

Arcellx

51-200 employees

Arcellx develops innovative cell therapies for cancer and autoimmune

Biotechnology

Compensation Overview

$235,000 - $260,000Annually

+ Annual Bonus + Equity (RSU) Grant + Relocation Assistance

Senior, Expert

San Carlos, CA, USA

Required Skills
Communications
Requirements
  • Bachelor's degree
  • 7-10+ years' experience working within GCP a regulated environment
  • Experience with GLP and GVP is a plus
  • Experience implementing and integrating clinical quality systems in CBER regulated biotechnology companies
  • Knowledge of applicable GCP regulations and industry guidance
  • Strong communication and presentation skills with good executive presence
Responsibilities
  • Develop and implement programs that support Arcellx’s GCP-regulated activities
  • Lead the GCP supplier management and oversight programs including developing audit schedules, performing audits and the creation of quality agreements
  • Represent Quality on clinical project teams and act as the GCP Quality lead for the oversight of all Quality aspects performed at Clinical Research Organizations (CROs) contract laboratories and clinical sites
  • Assist in the development and implementation of systems to ensure clinical adverse event reporting and tracking and robust data integrity programs
  • Support regulatory inspection (BIMO) readiness activities as it relates to any Arcellx phase II/ phase III clinical studies
  • Partner with the VP of Quality in creation of clinical quality department goals and metrics

Arcellx develops innovative cell therapies for cancer and autoimmune diseases, leveraging their novel D-Domain technology and transformative ddCAR and ARC-SparX platforms to enhance cell therapy.

Company Stage

N/A

Total Funding

$736M

Headquarters

Redwood City, California

Founded

2014

Growth & Insights
Headcount

6 month growth

9%

1 year growth

35%

2 year growth

76%