Senior / Principal Clinical Scientist, Clinical Development
Immunome, Inc.
August 29, 2026
Remote friendly (Bothell, WA)
United States
Clinical Research and Development
Position Overview
Senior/Principal Clinical Scientist, Clinical Development to design, execute, and interpret multiple oncology clinical trials.
Responsibilities
- Oversee clinical trial execution with scientific and regulatory rigor.
- Design and develop clinical trial protocols, informed consent forms, and study documents.
- Collaborate with principal investigators, key opinion leaders, and sites; serve as Lead Clinical Scientist for multiple trials.
- Support data generation/validation (CRF design; clinical data review/query resolution).
- Contribute to clinical study reports, regulatory submissions, and publications.
- Review site/CRA training materials and support SIV/Investigator meetings; assist study committee activities (e.g., DMC).
- Perform site-facing activities (training; responding to clinical questions).
- Participate in clinical development plan and timeline strategy.
- Present trial data to internal/external stakeholders (scientific advisory boards, regulatory agencies).
- Mentor/develop junior team members (potential for direct reports).
Qualifications
- PhD, MD, PharmD, or MS (or equivalent) in life sciences.
- 2+ years experience in clinical science/research (clinical development required); biotech/biopharma industry and oncology experience preferred.
- Strong leadership, project management, and communication skills.
- Travel may be required.
Knowledge and Skills
- Drug development process/study design and clinical operations expertise.
- Clinical trial data analysis software/tools.
- Data review, trend identification, and data interpretation.
- Regulatory knowledge (GCP, ICH, FDA).
- Analytical, organizational, and communication skills; fast-paced collaborative work; problem-solving and attention to detail.
Senior/Principal Clinical Scientist, Clinical Development to design, execute, and interpret multiple oncology clinical trials.
Responsibilities
- Oversee clinical trial execution with scientific and regulatory rigor.
- Design and develop clinical trial protocols, informed consent forms, and study documents.
- Collaborate with principal investigators, key opinion leaders, and sites; serve as Lead Clinical Scientist for multiple trials.
- Support data generation/validation (CRF design; clinical data review/query resolution).
- Contribute to clinical study reports, regulatory submissions, and publications.
- Review site/CRA training materials and support SIV/Investigator meetings; assist study committee activities (e.g., DMC).
- Perform site-facing activities (training; responding to clinical questions).
- Participate in clinical development plan and timeline strategy.
- Present trial data to internal/external stakeholders (scientific advisory boards, regulatory agencies).
- Mentor/develop junior team members (potential for direct reports).
Qualifications
- PhD, MD, PharmD, or MS (or equivalent) in life sciences.
- 2+ years experience in clinical science/research (clinical development required); biotech/biopharma industry and oncology experience preferred.
- Strong leadership, project management, and communication skills.
- Travel may be required.
Knowledge and Skills
- Drug development process/study design and clinical operations expertise.
- Clinical trial data analysis software/tools.
- Data review, trend identification, and data interpretation.
- Regulatory knowledge (GCP, ICH, FDA).
- Analytical, organizational, and communication skills; fast-paced collaborative work; problem-solving and attention to detail.