Cullinan Therapeutics is hiring a
Principal Scientist/Associate Director

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Cullinan Therapeutics

πŸ’΅ ~$110k-$135k
πŸ“Remote - United States

Summary

Join our team as a Senior Research Scientist to oversee and/or support early stage drug development projects in the Cullinan pipeline. You will lead contract research organizations, design program strategies, develop budget forecasts, and deliver impactful presentations. This role requires a PhD in cancer immunotherapy or related field with 1-3 years of industry experience.

Requirements

  • 1-3 years of industry experience
  • PhD in cancer immunotherapy, immunology, cancer biology, biological engineering, biochemistry, or a related field
  • Experience in cancer and/or immunology research, preferably with experience in immuno-oncology, autoimmunity and/or protein engineering
  • Experience evaluating drug asset value propositions, either in venture capital or in the biotech industry, is preferred
  • Innovative thinker
  • Strong attention to detail
  • Highly collaborative, with an interest in working within and across teams
  • Excellent verbal and written communication skills to serve as liaison between Cullinan and contract research organizations and other outward-facing partners
  • Ability to excel in a fast-paced work environment with focus on multiple programs in parallel

Responsibilities

  • Lead and oversee contract research organizations in discovery efforts
  • Design and execute program strategy and research plans
  • Develop budget forecasts for drug development programs
  • Day-to-day oversight of external research efforts
  • Deliver impactful presentations to share program updates and data with colleagues
  • Oversee logistical management of Cullinan samples
  • Lead internal technical discussions on preclinical programs
  • Develop innovative strategies to move existing programs forward
  • Lead internal innovation projects and generate ideas for new pipeline programs
  • Routinely review relevant scientific literature and competitive landscape; attend scientific conferences
  • Author/review regulatory submissions documents related to nonclinical IND-enabling studies
  • Participate in diligence activities to support the evaluation of potential new assets for addition to Cullinan portfolio

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