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Biotechnology Associate Director Jobs in Seattle, WA

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Biotechnology Associate Director information

What does a biotechnology associate director do?

A Biotechnology Associate Director oversees research and development projects within biotech organizations, ensuring that scientific and business objectives are met. They manage teams of scientists and technical staff, coordinate cross-functional projects, and are responsible for regulatory compliance and quality assurance. Additionally, they play a key role in strategic planning, budgeting, and communicating progress to senior leadership. Their work helps guide the company’s innovation pipeline and ensures that products move efficiently from concept to market.

What are the key skills and qualifications needed to thrive as a biotechnology associate director?

To thrive as a Biotechnology Associate Director, you need advanced knowledge in molecular biology or related life sciences, extensive research experience, and a graduate degree (often a Ph.D.) in biotechnology or a similar field. Familiarity with laboratory information management systems (LIMS), regulatory compliance standards (like FDA or EMA), and project management tools is typically required. Strong leadership, strategic thinking, and communication skills distinguish top performers in this role. These competencies are crucial for leading teams, ensuring regulatory compliance, and driving the successful development of innovative biotech solutions.

What are some common challenges biotechnology associate directors face when leading cross-functional teams?

Biotechnology Associate Directors often navigate the complexities of coordinating efforts between research scientists, regulatory affairs, manufacturing, and commercial teams. One common challenge is aligning diverse priorities and timelines while ensuring compliance with strict industry regulations. Effective communication and adaptability are essential to foster collaboration, resolve conflicts, and keep projects on track. Successfully managing these dynamics leads to efficient product development and positive team outcomes.

What is the difference between Biotechnology Associate Director vs Biotechnology Scientist?

AspectBiotechnology Associate DirectorBiotechnology Scientist
Required CredentialsMaster's or PhD in Biotechnology, Life Sciences, or related field; extensive industry experienceMaster's or PhD; focus on research and development
Work EnvironmentLeadership roles in R&D teams, project management, strategic planningLaboratory research, experimental design, data analysis
Employer & Industry UsageBiotech companies, pharmaceutical firms, biotech divisionsResearch institutions, biotech companies, academia
Common Search & ComparisonOften compared for leadership and strategic rolesFocused on scientific research and experimentation

The Biotechnology Associate Director typically holds a leadership position overseeing research teams and strategic projects, requiring extensive experience and advanced degrees. In contrast, a Biotechnology Scientist primarily conducts laboratory research and experiments. Both roles are vital in biotech companies, but they differ in responsibilities, focus, and career level.

What are popular job titles related to Biotechnology Associate Director jobs in Seattle, WA?

For Biotechnology Associate Director jobs in Seattle, WA, the most frequently searched job titles are:

What job categories do people searching Biotechnology Associate Director jobs in Seattle, WA look for?

The top searched job categories for Biotechnology Associate Director jobs in Seattle, WA are:

What cities near Seattle, WA are hiring for Biotechnology Associate Director jobs?

Cities near Seattle, WA with the most Biotechnology Associate Director job openings:

Biotechnology Associate Director jobs near you
Infographic showing various Biotechnology Associate Director job openings in Seattle, WA as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 24% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Associate Director / Director, Clinical Development

Immunome, Inc.

Bothell, WA • On-site

$342K - $394K/yr

Full-time

Re-posted 21 days ago

Job description

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 safetymonitoringand pharmacovigilance activities, including review and medical input on adverse events, suspected unexpected serious adverse reactions, and other clinically significant safety findings. 
  • Collaboratewith internal and external stakeholders to design andimplementa 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-functionallywith 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 keybiomarkerand pharmacodynamic endpoints into clinical study designs. 
  • Establish andmaintainstrongrelationships 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, investigatormeetings, and site trainings. 
  • Support quality initiatives related to clinical trial conduct,as needed. 

Qualifications

  • M.D., D.O., orequivalent. Board certification in medical oncologyorhematology preferred.  
  • A minimum of1year of experience in Clinical DevelopmentandPhase 1 - 3 oncology clinical trialsin 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 successfultrack recordin 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 

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