WHO WE ARE

Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We believe that cell therapies are one of the forward pillars of medicine and our mission is to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible.
Our team members are made up of talented innovators and dreamers working from our offices in Gaithersburg, Maryland, and Redwood City, California. At Arcellx, we hire exceptional people and create a fun, diverse, supportive, and informal environment that allows everyone to do their best work.

SKILLS AND EXPERIENCE WE LOOK FOR

• BA/BS in science-related field with 8+ years’ relevant work experience in oncology trials, with prior experience as a study lead.
• Strong knowledge of clinical research process, including working knowledge of all functional areas of clinical trials and regulatory requirements.
• Exceptional project management skills, organization, and problem-solving skills.
• Eager to learn with a collaborative, team-oriented mindset.
• Excellent written and verbal communication skills with an ability to express complex ideas to study personnel at research and clinical institutions.

• Oversees scope, quality, timelines, and budget with the internal functional leads, CRO, and vendors to ensure overall project objectives are met.
• Take a leadership role in the assigned study management activities.
• Provide study-specific training and leadership to clinical research staff.
• Anticipates obstacles or complex issues at the site, vendor, and study levels and implements solutions to achieve project goals or to overcome identified obstacles.
• Proactively identify issues for escalation, participate in problem-solving and implementation of risk mitigation.
• Lead other study activities as needed (e.g., site selection, start-up, recruitment, protocol deviation and TMF review).
• Develop and ensure compliance with clinical monitoring plan; conducts or oversees co-monitor as needed for staff training and quality assurance (QA) purposes.
• Review the quality and integrity of the clinical data through review of electronic CRF data.