Jobs · Analyst · Washington

Senior / Principal Clinical Scientist, Clinical Development

Immunome, Inc. · Bothell, WA · 3 days ago
Analyst$146k–$182k/yrFull-time

Responsibilities

  • Oversee the execution of clinical trials and ensure scientific and regulatory rigor.
  • Design and develop multiple clinical trial protocols, informed consent forms, and other study-related documents.
  • Collaborate with principal investigators, key opinion leaders, and clinical trial sites to ensure robust study design and execution.
  • Serve as Lead Clinical Scientist for multiple trials.
  • Conduct activities related to data generation and validation, including CRF design and clinical data review/query resolution.
  • Contribute to the preparation of clinical study reports, regulatory submissions, and publications.
  • Review development of site and CRA training materials and present at SIV and Investigator meetings and support on Study committee (e.g., DMC) activities.
  • Perform site-facing activities such as training and responding to clinical questions.
  • Participate in the strategic development of clinical development plans and timelines.
  • Present clinical trial data and findings to internal and external stakeholders, including scientific advisory boards and regulatory agencies.
  • Mentor and develop junior team members with potential to manage direct reports.

Qualifications

  • PhD, MD, PharmD, MS, or equivalent degree in life sciences.
  • A minimum of 2 years of experience in clinical science, clinical research, or equivalent; clinical development experience is required, biopharmaceutical/biotechnology industry and oncology experience preferred.
  • Strong leadership, project management, and communication skills.
  • Travel may be required.
  • Extensive experience in drug development process, study design, clinical operations.
  • Extensive experience in clinical trial data analysis software and tools.
  • Strong knowledge and skills to support program specific data review, trend identification, and data interpretation.
  • Strong understanding of regulatory requirements and guidelines for clinical trials (e.g., GCP, ICH, FDA).
  • Excellent analytical, organizational, and communication skills.
  • Ability to work effectively in a fast-paced, collaborative environment.
  • Strong problem-solving skills and attention to detail.

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