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Biotech Project Management Jobs in Bothell, WA (NOW HIRING)

RetinAI Medical

Client Executive - Full Time - USA

Seattle, WA · On-site

$87K - $118K/yr

A proven track record of consultative sales within Ophthalmology Pharma, Biotech, MedTech, or ... Solid project management and organizational skills, with hands-on proficiency in CRM platforms like ...

Variant Bio

Executive Administrator

Seattle, WA · On-site

... biotech, life sciences, or venture-backed company. Given the dynamic nature of a startup ... Manage special projects from inception through execution, often operating across teams and without ...

Variant Bio

Executive Administrator

Seattle, WA · On-site

... biotech, life sciences, or venture-backed company. Given the dynamic nature of a startup ... Manage special projects from inception through execution, often operating across teams and without ...

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Showing results 41-60

All JobsBiotech Project Management JobsBiotech Project Management Jobs in Bothell, WA

Biotech Project Management information

See Bothell, WA salary details

$43K

$114.8K

$181.1K

How much do biotech project management jobs pay per year?

As of Aug 6, 2026, the average yearly pay for biotech project management in Bothell, WA is $114,787.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,800.00 and $137,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in biotech project management?

To thrive in Biotech Project Management, you need a strong background in life sciences, experience in project planning and execution, and ideally a relevant degree (such as biology, biotechnology, or project management certification). Familiarity with project management software (like MS Project or Asana), regulatory compliance systems, and possibly certifications like PMP is often expected. Exceptional communication, leadership, problem-solving, and time management skills will help you stand out in this role. These competencies ensure projects remain on schedule, compliant, and collaborative in the fast-paced, highly regulated biotech industry.

What are the most common challenges faced by professionals in biotech project management?

Biotech Project Management professionals often juggle cross-disciplinary teams, tight timelines, and complex regulatory requirements, which can make prioritizing tasks a challenge. Navigating scientific uncertainties and adapting to project scope changes are daily realities given the fast pace of biotech innovation. Having strong organizational and people skills helps to manage competing priorities while keeping all stakeholders aligned. By mastering these challenges, professionals can significantly contribute to the timely advancement of vital scientific initiatives.

What is a biotech project management?

A Biotech Project Management job involves overseeing and coordinating research, development, and commercialization projects in the biotechnology industry. Project managers in this field ensure that scientific, regulatory, and business objectives are met on time and within budget. They work closely with cross-functional teams, including scientists, regulatory experts, and business stakeholders, to drive project success. Strong organizational, problem-solving, and communication skills are essential for managing risks and ensuring compliance with industry regulations.

What are popular job titles related to Biotech Project Management jobs in Bothell, WA? For Biotech Project Management jobs in Bothell, WA, the most frequently searched job titles are:
What job categories do people searching Biotech Project Management jobs in Bothell, WA look for? The top searched job categories for Biotech Project Management jobs in Bothell, WA are:
What cities near Bothell, WA are hiring for Biotech Project Management jobs? Cities near Bothell, WA with the most Biotech Project Management job openings:
Biotech Project Management jobs near you
Infographic showing various Biotech Project Management job openings in Bothell, WA as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $114,787 per year, or $55.2 per hour.

Associate Director / Director, Clinical Development

Immunome, Inc.

Bothell, WA

$342K - $394K/yr

Other

Posted 23 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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