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Clinical Development Biotech Jobs in Seattle, WA

Pfizer

Head of AI Clinical Excellence

Bothell, WA · On-site

$89K - $121K/yr

Lead development of AI-enabled approaches to improve clinical trial performance, operational ... MD and 4+ years of relevant experience within pharmaceutical, biotechnology, CRO, regulatory, or ...

Systimmune

Director, Clinical Data Management

Redmond, WA · On-site

$190K - $250K/yr

Oncology and/or antibody-drug conjugate (ADC) development experience. * Experience managing global clinical trials across multiple regions. * Prior experience in a growing biotechnology company.

Systimmune

Executive Director, Finance

Redmond, WA · On-site

$200K - $270K/yr

Required Qualifications and Behaviors : * 12+ years of progressive finance experience in biotech/pharma, with significant exposure to clinical development, R&D FP&A, and alliance finance in a biotech ...

SystImmune, Inc

Executive Director, Finance

Redmond, WA · On-site

$200K - $270K/yr

Required Qualifications and Behaviors : * 12+ years of progressive finance experience in biotech/pharma, with significant exposure to clinical development, R&D FP&A, and alliance finance in a biotech ...

Zymeworks

Senior Program Manager (Clinical)

Bellevue, WA · On-site

$105K - $161K/yr

Company Description Zymeworks is a global biotechnology company managing a portfolio of licensed ... Develop and implement a new matrixed Product Development Team framework with input from cross ...

Umoja Biopharma

Senior Medical Director

Seattle, WA · On-site

$270K - $333K/yr

Minimum of 5 years of clinical development experience, including at least 4 years in the biotechnology or pharmaceutical industry. * Demonstrated expertise in cell & gene therapy, ideally with CAR-T ...

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Clinical Development Biotech information

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How much do clinical development biotech jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for clinical development biotech in Seattle, WA is $61.85, according to ZipRecruiter salary data. Most workers in this role earn between $45.43 and $73.03 per hour, depending on experience, location, and employer.

What is clinical development in biotech?

Clinical development in biotech refers to the process of testing new drugs or therapies in human participants to determine their safety and effectiveness. This phase follows preclinical research and involves multiple stages of clinical trials, from Phase I (safety) to Phase III (efficacy and monitoring of side effects). Clinical development professionals coordinate the design, implementation, and analysis of these studies, ensuring compliance with regulatory standards. Their work is crucial in bringing innovative treatments from the laboratory to patients. Success in this field requires knowledge of medical science, regulatory guidelines, and project management.

What are the typical challenges faced by professionals working in clinical development within the biotech industry?

Professionals in clinical development for biotech companies often encounter challenges related to navigating complex regulatory requirements, managing tight timelines, and ensuring robust data quality across clinical trials. Additionally, frequent cross-functional collaboration is needed, as teams work closely with regulatory affairs, medical affairs, and data management to drive studies forward. Adapting to evolving scientific advancements and shifting project priorities are also common, so flexibility and strong communication skills are essential for success in this fast-paced environment.

What is the difference between Clinical Development Biotech vs Clinical Research Associate?

AspectClinical Development BiotechClinical Research Associate
Required CredentialsBachelor's or higher in life sciences, relevant certificationsBachelor's in life sciences, often with CRA certification
Work EnvironmentPharmaceutical/biotech companies, labs, clinical trial teamsMonitoring sites, clinical trial sites, sponsor offices
Employer & Industry UsageBiotech firms, pharmaceutical companies, CROsPharmaceutical companies, CROs, research organizations
Common Search & ComparisonYesYes

The Clinical Development Biotech role focuses on planning and managing clinical trials within biotech companies, often involving protocol development and regulatory submissions. In contrast, a Clinical Research Associate primarily monitors clinical trial sites to ensure compliance and data integrity. While both roles require similar educational backgrounds and certifications, their daily responsibilities and work environments differ, with the former being more involved in trial design and the latter in trial oversight.

What are the key skills and qualifications needed to thrive as a Clinical Development professional in biotech, and why are they important?

To thrive in Clinical Development within biotech, you need a strong background in life sciences, clinical trials management, and regulatory compliance, often supported by an advanced degree (e.g., PhD, PharmD, or MD). Proficiency with clinical trial management systems (CTMS), data analysis tools, and familiarity with ICH-GCP guidelines and FDA regulations are typically required. Strong project management, communication, and problem-solving skills help navigate complex studies and multidisciplinary teams. These competencies are essential to ensure safe, efficient, and compliant development of new therapies from concept to market.
What are popular job titles related to Clinical Development Biotech jobs in Seattle, WA? For Clinical Development Biotech jobs in Seattle, WA, the most frequently searched job titles are:
What job categories do people searching Clinical Development Biotech jobs in Seattle, WA look for? The top searched job categories for Clinical Development Biotech jobs in Seattle, WA are:
What cities near Seattle, WA are hiring for Clinical Development Biotech jobs? Cities near Seattle, WA with the most Clinical Development Biotech job openings:
Clinical Development Biotech jobs near you
Infographic showing various Clinical Development Biotech job openings in Seattle, WA as of July 2026, with employment types broken down into 8% Locum Tenens, 2% As Needed, 79% Full Time, 4% Part Time, 1% Temporary, and 6% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $128,651 per year, or $61.9 per hour.

Associate Director / Director, Clinical Development

Immunome, Inc.

Bothell, WA • On-site

$342K - $394K/yr

Full-time

Posted 19 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 submitted to the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-3050, an IND-cleared FAP-targeted radiotherapy; and IM-1617, an IND-cleared solid tumor ADC. 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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