Associate, Clinical Trial Management

๐Ÿข Lyellimmunopharma · ๐Ÿ“ Seattle, Washington, United States ๐Ÿ’ฐ $100,000 - $130,000 / yr
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Position Summary & Responsibilities

Using living cells to treat โ€“ and sometimes even cure โ€“ cancer is one of the most dramatic advances in modern medicine. Patients with hematologic malignancies have been successfully treated with cell therapies. However, these profound results have not yet been achieved in patients with solid tumors, representing approximately 90% of all cancers. And for patients with hematologic malignancies, there is a need for next-generation cell therapies that can deliver increased response rates and longer duration of response.  We are a clinical-stage company advancing a pipeline of next-generation CAR T-cell therapies for patients with solid tumors or hematologic malignancies. Lyellโ€™s product candidates are enhanced with novel technology designed to generate T cells that resist exhaustion and have qualities of durable stemness in order to drive durable tumor cytotoxicity and achieve consistent and long-lasting clinical response. We were founded by cell therapy pioneers whose decades of research elevated the broader understanding of T-cell biology and its interaction with cancer. In our quest to advance next-generation CAR T-cell therapies, we have built a fully integrated company capable of discovering new technologies, translating science into therapies, manufacturing cell therapy products, and clinically evaluating them in patients. Our culture is based on Science, Respect, Collaboration, and Courage and reflects who we are, the environment we create, and our mission's urgency. 

The incumbent is responsible for conducting tasks related to the trial, as assigned; escalates issues and recommends solutions to address concerns; with the guidance from the Director/Associate Director Clinical Operations/Senior Clinical Trial Manager.

KEY ROLE AND RESPONSIBILITIES:

  • Conducts tasks related to the trial as assigned; escalates issues and recommends solutions to address concerns
  • Develops tactical plans, detailed process steps and creates forms as needed for efficient trial execution; collaborates and seeks feedback from broader study team stakeholders to improve/optimize recommendations
  • Responsible for oversight of defined tasks with CRO partners; ensures deliverables are conducted on a timely, qualit
๐ŸŽฏ Candidate Preparation Guide For Lyellimmunopharma Applicants

Key Role Competencies & Evaluation Highlights

Key Role Focus:

Assessing rigorous scientific innovation, cell therapy manufacturing complexity, and uncompromising translational research standards.

๐Ÿ“‹ Preparation Priorities (Key Areas to Clarify):
  • 1. Hand-waving through complex CMC (Chemistry, Manufacturing, and Controls) or clinical hurdles
  • 2. Lack of urgency in accelerating life-saving therapies through the pipeline
  • 3. Working in academic isolation without appreciating cross-functional translation to clinical scale
โœจ Recommended Role Alignment Hook:

I bring rigorous translational science and scalable process development expertise to overcome the toughest barriers in cell therapy.

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