Arcellx

👥 101-250💰 $200,000,000 Post-IPO Equity over 1 year agoPharmaceuticalBiotechnologyBiopharmaLife ScienceHealth Care📈 Public Company
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Arcellx is a clinical-stage biotechnology company pioneering innovative cell therapies for cancer and other incurable diseases. Our lead product candidate, CART-ddBCMA, is in Phase 1 trials for multiple myeloma and has received FDA Fast Track, Orphan Drug, and Regenerative Medicine Advanced Therapy designations. We're also advancing our dosable and controllable CAR-T therapy, ARC-SparX, into clinical trials for multiple myeloma and acute myeloid leukemia. Arcellx is making significant strides in revolutionizing cell therapy, offering safer, more effective, and accessible treatments. We operate in a dynamic and rapidly evolving field, requiring a cutting-edge tech stack. Our team utilizes technologies such as Google Tag Manager, Google Font API, and leverages mobile-first design principles (iPhone/Mobile Compatible, Viewport Meta). We're committed to robust security (SSL by Default, SPF, DNSSEC, HSTS) and maintain a collaborative, innovative culture that values character, audacity, determination, collaboration, and originality. Our diverse and supportive environment empowers our employees to do their best work. Arcellx is a rapidly growing company with significant funding and a strong market position. We're a publicly traded company (NASDAQ: ACLX) with a workforce of 101-250 employees, dedicated to advancing humanity through safer and more effective cell therapies. We offer competitive salaries and benefits, including comprehensive health insurance, unlimited vacation, and generous parental leave. Join us in our mission to destroy cancer and advance humanity. Our commitment to excellence extends beyond our science. We cultivate a supportive and inclusive environment that fosters collaboration and innovation. Our teams are geographically distributed but highly connected, ensuring efficient communication and collaboration across projects.

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🔥 Medical Science Liaison
Posted about 1 month ago

💸 180000.0 - 225000.0 USD per year

🔍 Biotechnology

  • Advanced degree in health sciences (PharmD, M.D., or Ph.D. in a medically related field) preferred with 2-3 years of relevant experience in the hematologic malignancy therapeutic area and/or cell therapy is desired.
  • 2+ years of experience in MSL/Medical Affairs in relevant therapeutic area.
  • Familiarity/experience with healthcare systems and access environments.
  • Demonstrated ability to partner, influence, and work successfully within and across functions and levels of leadership.
  • Excellence in communication and presentations skills with strong personal integrity.
  • Ability to travel domestically approximately 50-70%.
  • Establish and maintain professional relationships with HCPs (MD, PA, NP, RN, PharmD) within the cell therapy and hematology space via both in-person and virtual interactions.
  • Develop and execute territory plans in alignment with Medical Affairs strategies, which includes interactions with academic thought leaders, disease state experts, cell therapy-referring HCPs, and community practices.
  • Compliantly partner with field-based teams to optimize HCP support and customer service.
  • Deliver approved medical and scientific education relevant to disease state and Arcellx products.
  • Share insights from external thought leaders and HCPs to inform the development of medical strategies and the development of future clinical programs.
  • Represent Arcellx at medical and scientific conferences.
  • Partner with clinical operations to support the execution of clinical trials.
Posted about 1 month ago
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🧭 Full-Time

💸 275000.0 - 305000.0 USD per year

🔍 Biotechnology

  • BSc in natural or health sciences (biology, pharmaceutical sciences, or equivalent).
  • 12-15+ years of clinical regulatory affairs experience, including early and late phase research, with strong knowledge of health authority regulations and guidance.
  • Proficiency directly writing submission documents that support clinical trials, marketing applications, and lifecycle management.
  • Experience interacting with Health Authorities and reviewing materials to ensure compliance with applicable regulatory laws and guidance.
  • Solid understanding of biology, chemistry and/or engineering relevant to pharmaceutical industry.
  • Exceptional project management skills, organizational and problem-solving skills.
  • Eager to learn with a collaborative, team-oriented mindset.
  • Excellent written and verbal communication skills.
  • Develop and execute global clinical regulatory strategies.
  • Lead program teams in preparing regulatory submissions including briefing documents, IND/CTA/BLA filings, and marketing applications.
  • Oversee strategy and drafting of documents related to interactions with regulatory authority on clinical matters.
  • Maintain detailed knowledge of global regulatory environment relevant for cell therapies and regenerative medicine.
  • Support internal clinical and development teams to provide direction on global regulations and guidance.
Posted 3 months ago
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