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Immunome Jobs in Renton, WA (NOW HIRING)

Immunome, Inc.

Director, Quality Operations

Bothell, WA · On-site

Company Overview Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of ...

Immunome, Inc.

Director, Toxicology

Bothell, WA · On-site

Company Overview Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of ...

Doist

Director, Clinical Development Systems

Bothell, WA · On-site

$229 - $256/hr

Company Overview Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of ...

Posted today

Immunome, Inc.

Director, Quality Operations

Bothell, WA · On-site

Position Overview The Director, Quality Operations will report to the Senior Director, Quality Assurance and provide strategic operational leadership and oversight across assigned programs related to ...

Immunome, Inc.

Director, Toxicology

Bothell, WA · On-site

Position Overview The Director, Toxicology provides scientific and strategic leadership for the nonclinical safety assessment of oncology therapeutics from discovery through commercialization. This ...

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Immunome information

What is the difference between Immunome vs Immunologist?

AspectImmunomeImmunologist
Required CredentialsTypically advanced degrees in biology, immunology, or related fields; research experienceMedical degree (MD or DO), residency in immunology or related specialty, board certification
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsHospitals, clinics, research institutions, academic settings
Employer & Industry UsageBiotech companies, research organizations, pharmaceutical industryHealthcare facilities, academic institutions, research hospitals

Immunome primarily refers to a biotech company specializing in immune system research, while an immunologist is a medical or research professional specializing in immune system diseases. The main difference lies in Immunome being an organization or entity, whereas an immunologist is a healthcare professional or researcher working within or outside such organizations.

What cities near Renton, WA are hiring for Immunome jobs? Cities near Renton, WA with the most Immunome job openings:
Immunome jobs near you
Infographic showing various Immunome job openings in Renton, WA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 92% Physical, and 8% Remote job distribution.

Medical Director / Senior Medical Director, Clinical Development

Immunome, Inc.

Bothell, WA • On-site

Full-time

Re-posted 2 days ago

Job description

Company Overview
Immunome is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. We are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Our pipeline includes varegacestat, an investigational gamma secretase inhibitor for which an NDA has been accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.
Position Overview
We are seeking a highly motivated physician to serve as Medical Monitor for the late-stage development of varegacestat, an investigational therapy being developed for desmoid tumors. This individual will provide medical oversight for global clinical studies and serve as a key member of the Clinical Development team, partnering closely with Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, Medical Writing, and Translational Medicine.
The Medical Monitor will be responsible for patient safety oversight, protocol implementation, investigator engagement, medical review of efficacy and safety data, and contribution to regulatory interactions. This position offers an opportunity to play a significant role in the registration and global development strategy of a potentially first-in-class therapy addressing a significant unmet medical need.
Responsibilities
Medical Monitoring and Patient Safety
  • Serve as the primary Medical Monitor for global clinical studies.
  • Provide ongoing medical review of safety, efficacy, and eligibility data.
  • Evaluate and assess serious adverse events (SAEs), adverse events of special interest (AESIs), and emerging safety signals.
  • Collaborate with Pharmacovigilance to ensure timely safety assessment, signal detection, and risk management activities.
  • Participate in Safety Review Committees, Data Monitoring Committees, and other governance forums as needed.
  • Ensure subject safety remains the primary consideration in study conduct and decision-making.

Clinical Trial Conduct
  • Provide medical oversight of study execution from initiation through database lock and study reporting.
  • Support protocol development, protocol amendments, informed consent forms, and study-related documents.
  • Review protocol deviations, eligibility questions, endpoint assessments, and other medically relevant study issues.
  • Partner with Clinical Operations to address site-level medical questions and enrollment challenges.
  • Assist with development and maintenance of study training materials.

Investigator and External Engagement
  • Serve as a primary medical contact for investigators and study sites.
  • Participate in investigator meetings, site initiation visits, and key study governance meetings.
  • Support interactions with key opinion leaders and external experts.
  • Contribute to advisory boards and scientific discussions relevant to the development program.

Data Review and Interpretation
  • Conduct ongoing review of accumulating safety and efficacy data.
  • Collaborate with Clinical Scientists and Biostatistics to identify trends, data quality issues, and emerging clinical insights.
  • Participate in blinded and unblinded data review activities as appropriate.
  • Contribute to interpretation of study results and preparation of clinical study reports, publications, and scientific presentations.

Regulatory and Cross-Functional Leadership
  • Support preparation of regulatory submissions and health authority interactions.
  • Contribute clinical input into briefing books, responses to regulatory questions, and inspection readiness activities.
  • Collaborate with Regulatory Affairs, Clinical Pharmacology, Translational Medicine, Biometrics, and Commercial colleagues to support integrated product development.
  • Present clinical updates and recommendations to internal governance committees and senior leadership.

Qualifications
  • MD, DO, or equivalent medical degree.
  • A minimum of 3+ years industry clinical development experience, or equivalent experience.
  • Board certification or training in Oncology, Hematology/Oncology, Internal Medicine, or a related specialty.
  • Experience serving as a Medical Monitor for interventional clinical trials.
  • Working knowledge of GCP, ICH guidelines, and global regulatory requirements.
  • Strong understanding of oncology drug development and clinical trial conduct.
  • Excellent communication, collaboration, and problem-solving skills.

Knowledge and Skills
  • Experience supporting Phase 2 and/or Phase 3 oncology studies.
  • Experience with rare diseases, sarcomas, or desmoid tumors.
  • Experience supporting regulatory submissions and health authority interactions.
  • Experience working within a matrixed, cross-functional environment.
  • Demonstrated ability to interpret complex clinical and safety data and translate findings into development recommendations.

Washington State Pay Range
$287,887-$394,941 USD
E/E/O
Immunome, Inc. is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.
E-Verify
Immunome, Inc. is a participant in E-Verify. Please review the following notices: E-Verify Participation Poster | Right to Work Poster (English) | Right to Work Poster (Spanish).

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