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Associate Director Information Security Jobs in Bothell, WA

AditiStaffing

Security Analyst

Bellevue, WA · Remote

... certified, IT Staffing firm in the US offering contract, contract-to-hire & direct hire career ... Description: 6-8 years of experience in information security / technology or related field.

Uw

Associate Director, HR

Seattle, WA

About this Opportunity The Associate Director serves as thedepartment's senior administrative ... History of working with confidential information and ability to take appropriate action.

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Showing results 21-40

All JobsAssociate Information Security JobsAssociate Director Information Security JobsAssociate Director Information Security Jobs in Bothell, WA

Associate Director Information Security information

See Bothell, WA salary details

$40.8K

$92.6K

$181.1K

How much do associate director information security jobs pay per year?

As of Sep 10, 2026, the average yearly pay for associate director information security in Bothell, WA is $92,581.00, according to ZipRecruiter salary data. Most workers in this role earn between $60,400.00 and $106,800.00 per year, depending on experience, location, and employer.

What is the difference between Associate Director Information Security vs Security Manager?

AspectAssociate Director Information SecuritySecurity Manager
CertificationsCISSP, CISM, CISACISSP, CISM, CISA
Work EnvironmentStrategic planning, policy development, leadership rolesOperational security, team management, incident response
Industry UsageCommon in large organizations, corporate sectorsWidely used across industries, including finance, healthcare

The Associate Director Information Security typically focuses on strategic security initiatives, policy development, and leadership within an organization, often overseeing teams and aligning security with business goals. In contrast, a Security Manager handles day-to-day security operations, incident response, and team management. Both roles require similar certifications and are integral to organizational security, but they differ mainly in scope and focus.

Infographic showing various Associate Director Information Security job openings in Bothell, WA as of June 2026, with employment types broken down into 94% Full Time, 5% Part Time, and 1% Temporary. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $92,581 per year, or $44.5 per hour.

Associate Director / Director, Clinical Development

Bothell, WA • On-site

Immunome, Inc.
Biotechnology Research and Development • 11 - 50 employees
Learn more about Immunome, Inc.external

$342K - $394K/yr

Full-time

Re-posted 28 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 join Immunome as Associate Director / Director, Clinical Development, supporting the development of our investigational oncology pipeline. This individual will provide medical and scientific oversight for 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 Sciences.
The Associate Director/Director will be responsible for supporting protocol design and implementation, patient safety oversight, medical monitoring of ongoing trials, investigator and site engagement, medical review of emerging safety and efficacy data, and contribution to regulatory and scientific interactions. This position offers an opportunity to play a meaningful role in shaping the clinical development strategy for novel therapies addressing significant unmet needs in oncology.
Responsibilities
  • Provide medical monitoring oversight for oncology clinical trials, including review of safety events, eligibility questions, dose modifications, protocol deviations, laboratory abnormalities, and emerging clinical data.
  • Serve as the primary medical point of contact for investigators, study sites, CRO medical monitors, and internal cross-functional teams.
  • Support safety monitoring and pharmacovigilance activities, including review and medical input on adverse events, suspected unexpected serious adverse reactions, and other clinically significant safety findings.
  • Collaborate with internal and external stakeholders to design and implement a clinical development plan across indications.
  • Author key clinical trial documents and clinical sections of regulatory filings such as protocols, pre-INDs, IND/CTAs, Investigator Brochures, briefing documents, and BLAs.
  • Collaborate cross-functionally with clinical operations, regulatory, project management, manufacturing, and business development to define timelines, manage risks, and ensure milestone delivery.
  • Work closely with translational sciences to integrate key biomarker and pharmacodynamic endpoints into clinical study designs.
  • Establish and maintain strong relationships with PIs, KOLs, and other external stakeholders.
  • Review, assess, interpret, and communicate clinical trial data to internal stakeholders and external partners.
  • Lead clinical trial data publication efforts.
  • Lead or contribute to key external meetings such as advisory boards, safety review committees, investigator meetings, and site trainings.
  • Support quality initiatives related to clinical trial conduct, as needed.

Qualifications
  • M.D., D.O., or equivalent. Board certification in medical oncology or hematology preferred.
  • A minimum of 1 year of experience in Clinical Development and Phase 1 - 3 oncology clinical trials in a biotech or pharmaceutical setting, or equivalent.

Knowledge and Skills
  • Proven experience advancing therapeutic programs in early or late-stage clinical development.
  • Understanding of FDA and other health authority regulatory requirements and successful track record in regulatory interactions.
  • Demonstrated leadership and ability to effectively manage cross-functional teams.
  • Excellent written and verbal communication skills, with the ability to communicate complex medical and scientific information clearly to diverse audiences.
  • Strong organizational skills and ability to manage multiple studies, priorities, and timelines in a fast-paced biotech environment.
  • High attention to detail, sound clinical judgment, and strong commitment to patient safety and data quality.

Washington State Pay Range - Associate Director: $287,887 - $333,496
Washington State Pay Range - Director: $342,540 - $394,941
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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