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Contract Research Associate Jobs in Seattle, WA (NOW HIRING)

The Research Associate, Analytical Sciences will support drug substance and drug product ... Responsibilities also include support and management of external CDMO and contract test lab method ...

The Research Associate, Analytical Sciences will support drug substance and drug product ... Responsibilities also include support and management of external CDMO and contract test lab method ...

Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts ... Market research companies that partner with us will use questionnaires to identify and target ...

New

Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts ... Market research companies that partner with us will use questionnaires to identify and target ...

New

Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts ... Market research companies that partner with us will use questionnaires to identify and target ...

New

Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts ... Market research companies that partner with us will use questionnaires to identify and target ...

New

Product Testers are wanted to work from home nationwide in the US to fulfill upcoming contracts ... Market research companies that partner with us will use questionnaires to identify and target ...

New

Hospitality Associate

Seattle, WA ยท On-site

$200K - $250K/yr

Draft and negotiate IT/IS agreements and other commercial contracts. * Collaborate with attorneys ... Strong research, writing, and communication skills. * Team player with a client-centric approach.

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Contract Research Associate information

See Seattle, WA salary details

$18

$37

$53

How much do contract research associate jobs pay per hour?

As of Aug 3, 2026, the average hourly pay for contract research associate in Seattle, WA is $37.03, according to ZipRecruiter salary data. Most workers in this role earn between $29.81 and $42.12 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Contract Research Associate, and why are they important?

To thrive as a Contract Research Associate, you need a solid background in life sciences or a related field, attention to detail, and experience with clinical research processes. Familiarity with regulatory systems like FDA guidelines, Good Clinical Practice (GCP), data management tools, and electronic data capture (EDC) systems is typically required. Strong organizational skills, effective communication, and the ability to work independently or in teams help set candidates apart. These competencies ensure that clinical trials are conducted accurately, compliantly, and efficiently, supporting successful research outcomes.

What is the difference between Contract Research Associate vs Clinical Research Coordinator?

AspectContract Research AssociateClinical Research Coordinator
CredentialsBachelor's degree, often in life sciences; certifications like CCRP beneficialBachelor's degree in health sciences or related field; certifications like CCRP or CCRC advantageous
Work EnvironmentTypically in pharmaceutical or biotech companies, contract research organizations (CROs)Usually in hospitals, clinics, or research sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, academic medical centers, research institutions
Common Search & ComparisonYesYes

While both roles support clinical trials, a Contract Research Associate primarily works for pharmaceutical or biotech companies managing trial processes remotely or at sites, often on a contractual basis. A Clinical Research Coordinator typically works directly at research sites, coordinating patient visits and data collection. Both roles require similar credentials and certifications, but their work environments and employer types differ.

What are some typical challenges faced by Contract Research Associates when managing multiple studies simultaneously?

Contract Research Associates often juggle several clinical trials at once, which can pose challenges in time management and prioritization. Balancing the requirements of different sponsors, adhering to varying protocols, and ensuring accurate documentation for each study demand strong organizational skills. Additionally, staying up to date with regulatory changes and effective communication with site staff are crucial to avoid delays and ensure compliance. Developing efficient workflows and leveraging project management tools can help address these challenges.

What is a Contract Research Associate?

A Contract Research Associate (CRA) is a professional who is typically hired on a contractual basis to support and manage clinical trials or research projects. Their primary responsibilities include monitoring research sites, ensuring compliance with protocols and regulations, collecting and verifying data, and maintaining proper documentation. CRAs play a critical role in ensuring the integrity and safety of clinical studies, often working for pharmaceutical companies, contract research organizations (CROs), or academic institutions. The contract nature of the role means that assignments are usually project-based and may vary in duration and scope.
What are the most commonly searched types of Contract Research jobs in Seattle, WA? The most popular types of Contract Research jobs in Seattle, WA are:
What are popular job titles related to Contract Research Associate jobs in Seattle, WA? For Contract Research Associate jobs in Seattle, WA, the most frequently searched job titles are:
What job categories do people searching Contract Research Associate jobs in Seattle, WA look for? The top searched job categories for Contract Research Associate jobs in Seattle, WA are:
Infographic showing various Contract Research Associate job openings in Seattle, WA as of July 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $77,028 per year, or $37 per hour.

Research Associate I

Omeros Corp.

Seattle, WA โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 25 days ago


Job description


We are a fast-growing and dynamic organization seeking a Research Associate, Analytical Sciences to join our CMC team. The Research Associate, Analytical Sciences will support drug substance and drug product physicochemical and biophysical testing for Analytical Sciences (AS) and CMC activities. This individual will be part of a growing team responsible for the development, execution, and data analyses of liquid chromatography (LC), capillary electrophoresis (CE), spectroscopic, and compendial methods supporting clinical and commercial products.
The Research Associate will develop, execute, and manage methods used for clinical and commercial testing to support CMC, Discovery, Quality Assurance, Regulatory Affairs, and corporate objectives. The scope of this role includes laboratory testing support for all phases of product development, including clinical and commercial programs, with emphasis on biologics identity, purity, physicochemical, and compendial methods used for in-process, Release, Stability, comparability, and extended characterization testing. Responsibilities also include support and management of external CDMO and contract test lab method transfers, testing, troubleshooting, and investigations. This role will also support internal laboratory management activities.
Good things are happening at Omeros!
Who is Omeros?
Omeros is an innovative biotechnology company that discovers and develops first-in-class protein and small-molecule therapeutics for both large-market and orphan indications, with a focus on complement-mediated diseases, cancers, and addictive or compulsive disorders. Omeros' lead complement inhibitor YARTEMLEAยฎ (narsoplimab-wuug), which targets the lectin pathway's effector enzyme MASP-2, is FDA-approved and commercially available in the U.S. for the treatment of hematopoietic stem cell transplant-associated thrombotic microangiopathy (TA-TMA) in adult and pediatric patients aged two years and older. OMS1029, Omeros' long-acting MASP-2 inhibitor, has successfully completed Phase 1 clinical trials.
Under a recently announced asset purchase and licensing agreement, Novo Nordisk acquired global rights to zaltenibart (formerly OMS906), an inhibitor of MASP-3, the alternative pathway's key activator, which is in clinical development for PNH and other alternative pathway indications, along with associated intellectual property and related assets. Omeros' pipeline also includes OMS527, a phosphodiesterase 7 inhibitor in clinical development for cocaine use disorder, which is fully funded by the National Institute on Drug Abuse, and a growing portfolio of novel recombinant antibodies targeting multidrug-resistant organisms and novel molecular and cellular therapeutic programs for oncology. For more information about Omeros and its programs, visit www.omeros.com.
What are your job responsibilities?
  • Execute LC, CE, and other physicochemical testing to support CMC program activities
  • Develop and qualify LC, CE, and other physicochemical analytical methods
  • Author and review test methods, qualification protocols, and technical reports
  • Present experimental designs and results at AS, internal cross-functional, and external meetings
  • Support external test lab documentation and data review
  • Support lab management activities including equipment maintenance scheduling, testing calendar scheduling, inventory management, shipping and receiving, and waste disposal.
  • Ensure test methods development and execution activities are conducted in accordance with applicable regulatory requirements, internal policies, scientific standards, and project timelines

What education and experience do you need?
  • Science related Bachelor degree, or MS degree with 2+ years of laboratory experience; pharmaceutical or biotechnology industry experience preferred.
  • Hands-on experience with HPLC/UPLC (CEX, RP, SEC), CE (icIEF, CE-SDS), and other spectroscopic method used for protein therapeutic testing
  • Knowledge of cGMP requirements, ICH guidelines, regulatory expectations, and data integrity requirements preferred.
  • Proficiency with MS Office, Word, PowerPoint, and Excel software is required
  • Experience with laboratory notebooks is required
  • Data Sciences and statistical experience with software packages such as Minitab or JMP is preferred

Behavioral Competencies Required:
  • Demonstrated ability to build and maintain positive, collaborative relationships with management, peers, subordinates, cross-functional teams, and external contract organizations
  • Strong scientific judgment and ability to make sound technical decisions in relevant situations
  • Excellent written and oral communication skills, with the ability to clearly communicate complex scientific concepts to technical and non-technical audiences
  • Strong organizational, problem-solving, and decision-making skills with the ability to manage multiple priorities in a fast-paced environment
  • Self-motivated and detail-oriented, with the highest integrity and commitment to quality, compliance, and scientific excellence

Compensation and Benefits:
Omeros is proud to offer a competitive total compensation package designed to support the lives of our employees and their families. The wage scale for this position is ($65,000 - $85,000). Salaries will be determined based on knowledge, skills, education, and experience relevant to the role. Employees are offered medical, dental, vision, life insurance, and a 401(k) plan with a company match. Employees accrue three weeks of vacation and 80 hours of sick time on an annual basis and receive twelve paid holidays throughout the calendar year. This position is eligible for incentive and stock options. To learn more about Omeros, please visit www.omeros.com.
Omeros is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to status as a protected veteran or a qualified individual with a disability, or other protected status such as race, religion, color, national origin, sex, age, marital status, or any other factor determined to be unlawful by federal, state, or local statutes.
It is our policy to provide reasonable accommodation to anyone with a disability who needs assistance completing the job application process. If you need assistance, you can either send an e-mail to hr@omeros.com or contact Omeros, asking for Human Resources, at (206) 676-5000.

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About Omeros

Sourced by ZipRecruiter

Industry

Biotechnology research and development

Company size

201 - 500 Employees

Headquarters location

Seattle, WA, US

Year founded

1994

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