Job Details

Overview

Arcellx is a public, clinical-stage biotechnology company reimagining cell therapy by engineering innovative immunotherapies for patients with cancer and other incurable diseases. We aim to destroy cancer and advance humanity by developing cell therapies that are safer, more effective, and more broadly accessible. Our offices are in Gaithersburg, Maryland, and Redwood City, California. We hire exceptional people and foster a fun, diverse, supportive, and informal environment that enables everyone to do their best work.

What Matters to Us

Living our core values is essential to a high-performing, inclusive, and collaborative work environment. We look for candidates who demonstrate strong values alignment and bring diverse backgrounds, viewpoints, and abilities to the team.

Arcellx Core Values

• Start with authenticity: We foster an inclusive environment where each person can bring their authentic self to work.
• Think we before me: We prioritize collective success, collaborating and supporting one another to achieve our shared goals.
• Embrace the challenge: We deliver exceptional results by working with shared determination and a commitment to doing whats right.

Role

The role Senior Clinical Trial Manager (CTM)

You will be accountable for the day-to-day study management and successful delivery of our clinical trials. By managing all aspects of the study including budget and timeline, you will play a critical role in advancing our therapy through the clinic and to patients.

Responsibilities

• Oversee scope, quality, timelines, and budget with internal functional leads, CROs, and vendors to ensure study objectives are met.
• Lead assigned study management activities and provide study-specific training and leadership to clinical research staff.
• Anticipate obstacles at site, vendor, and study levels and implement solutions to achieve project goals.
• Proactively identify issues for escalation, participate in problem-solving, and implement risk mitigation.
• Lead additional study activities as needed (e.g., site selection, start-up, recruitment, protocol deviations, and TMF review).
• Develop and ensure compliance with the clinical monitoring plan; conduct or oversee co-monitoring for staff training and QA purposes.
• Review the quality and integrity of clinical data through review of electronic CRF data.

Qualifications

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

Rewards and Benefits

We value our people and support their well-being as part of delivering on our mission. Our compensation package includes a base salary, annual bonus based on company goals, and equity (RSU) grant. Relocation assistance is available if required. Our market-leading benefits include 100% medical, dental, and vision coverage for team members and dependents, unlimited vacation, a 3-day weekend every month, fully-paid parental leave for up to 6 months, tuition reimbursement, 401(k) employer contribution, and more.

Base salary range: $165,000 $200,000 per year. Where you fall in the range is determined by factors such as years of experience.

Join us in reimagining cell therapy and destroying cancer. For more on our technology, culture, and team, visit www.arcellx.com.