Senior ADME Scientist - Oncology ADCs

Immunomeinc; Bothell (WA); On-site; USD 150,000 - 204,000; Full time

Job summary

Immunome, Inc. in Washington state is seeking an experienced Senior Scientist II in ADME to lead the design and execution of nonclinical PK/PD and ADME programs, shaping candidate selection and regulatory submissions.

You will collaborate with cross-functional teams to integrate ADME insights into program strategy, mentor scientists, and stay current with evolving regulatory expectations.

The role offers a competitive salary and growth within a clinical-stage oncology portfolio leveraging ADCs.

Qualifications

• PhD in a relevant discipline with 0–3 years of industry experience in ADME/PKPD and ADME.
• Experience with ADCs required; additional experience with small molecules, monoclonal antibodies, or other modalities preferred.
• Hands-on expertise in PKPD modeling, PK/TK analysis, and study design.
• Knowledge of both non-regulated and regulated bioanalysis.

Responsibilities

• Perform modeling and simulation, analyze PKPD and PK/TK data, and provide clear interpretation to inform program decisions.
• Design and execute stage-appropriate PKPD and ADME studies to support candidate selection, clinical development, and regulatory submissions.
• Collaborate with cross-functional teams to ensure integration of ADME considerations into program strategy and timelines.
• Participate in Translational Sciences and Development team activities, contributing scientific expertise in ADME.
• Represent the ADME function at internal and external meetings, communicating timelines, data, and implications effectively.
• Maintain awareness of evolving best practices and regulatory expectations in ADME sciences.

Skills

Problem-solving skills

Excellent communication

Collaborative work style

Education

PhD in a relevant discipline

MS with 5+ years relevant industry experience

Job description

Immunome, Inc. in Washington state is seeking an experienced Senior Scientist II in ADME to lead the design and execution of nonclinical PK/PD and ADME programs, shaping candidate selection and regulatory submissions.

You will collaborate with cross-functional teams to integrate ADME insights into program strategy, mentor scientists, and stay current with evolving regulatory expectations.

The role offers a competitive salary and growth within a clinical-stage oncology portfolio leveraging ADCs.