1

Pharma Data Analyst Jobs in Seattle, WA (NOW HIRING)

Finance Business Analyst

Seattle, WA · On-site

$100K - $110K/yr

Analyze incoming data sets and develop detailed requirements around sourcing solutions, identify ... Pharma, Banking, Finance, etc. Our goal is to develop a long-term partnership with businesses and ...

Oversee GMP clinical and commercial stability planning, execution, statistical data analysis and ... Experience in big pharma/biotech; experience in a startup biopharma company is desirable

next page

Showing results 1-20

Pharma Data Analyst information

See Seattle, WA salary details

$38.7K

$94K

$154.8K

How much do pharma data analyst jobs pay per year?

As of Aug 29, 2026, the average yearly pay for pharma data analyst in Seattle, WA is $94,047.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,100.00 and $110,400.00 per year, depending on experience, location, and employer.

What does a Pharma Data Analyst do?

A Pharma Data Analyst collects, processes, and interprets data related to pharmaceuticals, including clinical trials, sales, and market trends. They use statistical tools and data visualization techniques to identify patterns and insights that support decision-making in drug development, regulatory compliance, and business strategy. Their role helps improve patient outcomes, optimize drug production, and drive business growth.

What are the key skills and qualifications needed to thrive as a Pharma Data Analyst?

To thrive as a Pharma Data Analyst, you need strong analytical skills, a background in life sciences or related fields, and proficiency in statistics and data interpretation. Familiarity with tools such as SQL, SAS, Python, or R, as well as experience with clinical trial databases and certifications like SAS Certified Specialist, are often expected. Excellent attention to detail, effective communication, and the ability to work collaboratively across multidisciplinary teams are valuable soft skills. These competencies ensure accurate analysis and reporting, drive data-driven decisions, and support regulatory compliance in the pharmaceutical industry.

What are some typical challenges Pharma Data Analysts face on the job?

Pharma Data Analysts often work with large, complex datasets from clinical trials and real-world evidence, which can present challenges in data integration, cleaning, and ensuring data quality. Additionally, analysts must stay current with evolving industry regulations and standards for data reporting, such as those from the FDA or EMA. Collaborating across different departments—such as clinical research, regulatory affairs, and biostatistics—requires strong communication skills and adaptability. These challenges offer opportunities to develop advanced technical expertise and deepen understanding of drug development processes.

How to become a pharmaceutical data analyst?

To become a pharmaceutical data analyst, typically a bachelor's degree in fields like statistics, biology, or data science is required. Developing skills in data analysis tools such as SQL, Excel, and statistical software, along with knowledge of the pharmaceutical industry, is essential. Gaining experience through internships or entry-level roles can also improve job prospects.

What are the most commonly searched types of Pharma Data Analyst jobs in Seattle, WA?

The most popular types of Pharma Data Analyst jobs in Seattle, WA are:

What job categories do people searching Pharma Data Analyst jobs in Seattle, WA look for?

The top searched job categories for Pharma Data Analyst jobs in Seattle, WA are:

Infographic showing various Pharma Data Analyst job openings in Seattle, WA as of August 2026, with employment types broken down into 87% Full Time, and 13% Contract. Highlights an 41% In-person, 14% Hybrid, and 45% Remote job distribution, with an average salary of $94,047 per year, or $45.2 per hour.

QC Chemist IV (Method Tranfer, Method Validation) / Pharma Industry

Bothell, WA • On-site

Contractor

Re-posted 2 days ago


Job description

Position Details:
Our client, a world-leading Pharmaceutical Company in Bothell, WA is currently looking for a QC Chemist IV to join their expanding team.
Job Title: QC Chemist IV (Method Tranfer, Method Validation) / Pharma Industry
Duration: 12 months contract, extendable up to 48 months
Location: Bothell, WA
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:

Quality Control Chemist

Role Summary:
This position serves as a quality control expert within the Quality Control Sciences and Validation group, providing critical support for analytical method transfer and validation activities across global pharmaceutical operations. 
The role requires an individual contributor who can independently manage complex technical projects while ensuring compliance with current Good Manufacturing Practices and regulatory standards. 
This scientist will serve as a technical authority for method transfer initiatives, working across multiple internal and external testing sites to support drug development programs. 
The position demands strong analytical expertise combined with excellent project management capabilities to coordinate deliverables and maintain timelines. 
Success in this role requires the ability to balance multiple priorities while maintaining rigorous attention to detail and scientific integrity throughout all validation and transfer activities.
 
Responsibilities:
Support Project Leads for method transfer and validation activities internally and externally for assigned pharmaceutical development programs
Author and review protocols and reports for method transfer, method validation, method bridging, and other technical development documentation associated with analytical methods
Plan and track method transfer and validation deliverables to ensure timely completion of project milestones
Collaborate and interact with internal global quality control testing sites and laboratories, external testing sites, project leads, and functional representatives
Review method transfer and validation assays, perform data verification, conduct non-routine data mining, and execute in-depth data analysis
Represent quality control in intra-department projects and initiatives or cross-functional teams in support of program and company goals
 
Skills:
Expertise in designing and evaluating method validation and transfer studies including partial re-validation, co-validation, and cross-validation approaches
Technical writing skills for authoring analytical methods, validation protocols, and transfer study reports
Expert knowledge of scientific principles and expertise with monoclonal antibodies, antibody-drug conjugates, vaccines, and gene therapy products
Strong analytical mindset and technical skills in analytical methods and plate-based methods, with preference for analytical separation method experience including size exclusion chromatography, imaged capillary isoelectric focusing, and capillary electrophoresis sodium dodecyl sulfate
Project management skills with demonstrated experience managing multiple projects simultaneously
Strong data interpretation, method troubleshooting skills, and sound scientific judgment
Excellent time management skills with attention to detail and commitment to achieving team and individual goals
Strong communication skills to lead teams and influence leaders or cross-functional team members
Understanding of regulatory guidance and requirements pertaining to method transfer, method validation, and regulatory submissions
 
Experience:
8-10 years of relevant experience in pharmaceutical or biological drug product development, analytical chemistry, or quality control within a regulated biotechnology or pharmaceutical company
Progressive levels of responsibility throughout career demonstrating increasing technical and leadership capabilities
 
Qualifications:
Bachelor's degree in analytical chemistry, biology, biochemistry, pharmaceutical science, or related technical discipline in life sciences
Post-graduate degree in a related field is preferred
This is an exceptional opportunity to join a leading pharmaceutical organization where you will play a pivotal role in ensuring the quality and regulatory compliance of critical analytical methods that support life-saving therapies. 
You will work at the intersection of science and quality, collaborating with talented professionals across global sites while contributing to innovative drug development programs that make a real difference in patients' lives.