ZipRecruiter

Log In

1

Clinical Data Associate Jobs in Renton, WA (NOW HIRING)

Immunome, Inc.

Clinical Trial Associate

Bothell, WA · On-site

$37.50 - $51.25/hr

Position Overview Immunome is seeking a Clinical Trial Associate (CTA) to support the operational ... Participate in the data cleaning activities as directed by Clinical Operations Manager. Vendor and ...

Impress

Sales Associate

Seattle, WA · On-site

$28 - $35/hr

As a Sales Associate / Treatment Coordinator, you are the key closer in our clinics. You will ... Enter all clinical data timely into patient's records and update internal channels (GoogleChat ...

New

Natera

Associate Clinical Oncology Specialist

Tacoma, WA · On-site

$110K - $130K/yr

The Associate Clinical Oncology Specialist (ACOS) is responsible for contributing to account sales ... Fluent in understanding data spreadsheets and technologies, although the Patient Retention ...

Tenacity Solutions LLC

Be Seen First

Clinical Research Associate

North Bethesda, MD · On-site

$115K - $135K/yr

Source data verification * CAPA development * Risk-based monitoring * Experience monitoring multi ... Certified Clinical Research Associate (CCRA) through ACRP or equivalent certification. * Previous ...

New

NWRPros

Clinical Research Associate

Seattle, WA · On-site

$115K - $145K/yr

As Clinical Research Associate (CRA) you will be primarily responsible for the operational ... Reviewing completed CRFs and data listings for accuracy, overseeing data discrepancy management ...

Tasso

Clinical Research Coordinator 2

Seattle, WA · On-site

$75K - $90K/yr

This position will report to our Associate Director, Clinical Operations. An ideal candidate will ... Enter and validate study data, e.g., into electronic data capture (EDC) platforms or study ...

Tasso

Clinical Research Coordinator 2

Seattle, WA · On-site

This position will report to our Associate Director, Clinical Operations. An ideal candidate will ... Enter and validate study data, e.g., into electronic data capture (EDC) platforms or study ...

previous pagenext page

Showing results 21-40

All JobsClinical Data Associate JobsClinical Data Associate Jobs in Renton, WA

Clinical Data Associate information

See Renton, WA salary details

$15

$43

$98

How much do clinical data associate jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for clinical data associate in Renton, WA is $43.99, according to ZipRecruiter salary data. Most workers in this role earn between $33.12 and $43.99 per hour, depending on experience, location, and employer.

What are some common challenges faced by clinical data associates when ensuring data quality during clinical trials?

Clinical Data Associates often encounter challenges such as identifying and resolving discrepancies in large datasets, maintaining strict compliance with regulatory standards, and coordinating timely data entry from multiple sites. They must work closely with clinical research teams and data managers to clarify ambiguous data and implement data cleaning procedures. Staying organized and detail-oriented is essential to ensure data accuracy and the successful progression of clinical trials.

What are the key skills and qualifications needed to thrive as a clinical data associate, and why are they important?

To thrive as a Clinical Data Associate, you need a solid understanding of clinical research, data management principles, and attention to detail, often supported by a degree in life sciences or a related field. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory guidelines like GCP or CDISC is typically required. Strong organizational skills, analytical thinking, and clear communication set outstanding candidates apart in this role. These skills ensure the accuracy, integrity, and compliance of clinical trial data, which are crucial for successful research outcomes and regulatory approval.

What does a clinical data associate do?

A Clinical Data Associate is responsible for collecting, validating, and managing clinical trial data to ensure its accuracy, completeness, and compliance with regulatory standards. They work closely with clinical research teams to monitor data quality, resolve discrepancies, and prepare data for analysis. Their work is essential in supporting drug development and regulatory submissions by ensuring reliable and high-quality clinical data.

What does a clinical data associate do?

A clinical data associate is responsible for tracking data and results in a research study. As a clinical data associate, your job duties are to collect data, perform data management, and input data into any software used by your team. You work on a research team, so you must be able to work collaboratively and have excellent organizational skills. While you spend most of your time in an office, you may be required to work in the field to record data. The only universal qualifications needed for this career are a background in health care or medical science research and experience with data management software like Oracle Clinical, Microsoft Excel, and SPSS.

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

AspectClinical Data AssociateClinical Research Coordinator
Primary RoleManage and ensure accuracy of clinical trial dataOversee trial operations, patient recruitment, and site management
CredentialsBachelor's in life sciences or related field; familiarity with data managementBachelor's in health sciences or related field; clinical trial experience
Work EnvironmentData management teams, clinical trial databasesClinical sites, hospitals, research facilities
Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

While both roles support clinical trials, a Clinical Data Associate primarily focuses on managing and validating trial data, ensuring accuracy and compliance. In contrast, a Clinical Research Coordinator handles the overall trial operations, including patient recruitment and site coordination. Both roles require relevant certifications and work within the clinical research industry, but their daily responsibilities differ significantly.

More about Clinical Data Associate jobs
What are the most commonly searched types of Clinical Data jobs in Renton, WA? The most popular types of Clinical Data jobs in Renton, WA are:
What job categories do people searching Clinical Data Associate jobs in Renton, WA look for? The top searched job categories for Clinical Data Associate jobs in Renton, WA are:
What cities near Renton, WA are hiring for Clinical Data Associate jobs? Cities near Renton, WA with the most Clinical Data Associate job openings:
Clinical Data Associate jobs near you
Infographic showing various Clinical Data Associate job openings in Renton, WA as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $91,505 per year, or $44 per hour.

Associate Director / Director, Biostatistics

Immunome, Inc.

Bothell, WA • On-site

$235K - $263K/yr

Full-time

Re-posted 13 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 accepted by the U.S. FDA; IM-1021, a clinical-stage ROR1 ADC; IM-1617, a clinical-stage solid tumor ADC; and IM-3050, a clinical-stage FAP-targeted radioligand therapy. We are also advancing a broad portfolio of early-stage ADCs pursuing undisclosed solid tumor targets.
Position Overview
The Associate Director / Director, Biostatistics provides statistical support to clinical studies, including the design, analyses, and interpretation of clinical trials. This position collaborates closely with cross-functional teams and provides scientifically rigorous statistical expertise on projects and protocols in support of clinical development and for publication and presentation.
Responsibilities
  • Apply rigorous statistical expertise to study design, statistical analysis plans, interpretation of results, project development plans, and regulatory issues.
  • Provide strategic statistical input into clinical development plans and study-level decision-making, anticipating downstream regulatory and data implications to inform study design and overall development strategy.
  • Plan, deliver, and communicate statistical analyses and scientific reports, including clinical trial and exploratory analyses, and support publications and scientific presentations.
  • Own the timeliness and quality of study- and submission-level statistical deliverables on assigned projects. For outsourced studies, manage vendors and monitor their performance and adherence to project timelines.
  • Ensure all study- and project-level statistical activities are conducted in compliance with relevant regulatory requirements (e.g., FDA regulations).
  • Contribute to interactions with regulatory authorities (e.g., FDA, EMA), including statistical input for regulatory meetings, responses to health authority questions, and preparation for advisory committee meetings.
  • Collaborate with internal partners (e.g., clinical development, clinical data management, statistical programming) to provide statistical support and help identify and resolve data issues.
  • Develop and lead initiatives in process improvement, training, and standard development.
  • Support ad hoc analyses and develop and validate programs for data analysis, reporting, and visualization.

Qualifications
  • PhD or Master's in Biostatistics, Statistics, or a related field.
  • A minimum of 6 years (with a PhD) or 8 years (with a Master's) of biostatistics experience supporting clinical trials in the pharmaceutical, biotech, or CRO industry, or equivalent.
  • A minimum of 2 years of leadership or people-management experience is preferred.

Knowledge and Skills
  • Prior oncology clinical trial experience, including familiarity with standard response criteria (e.g., RECIST 1.1), oncology endpoints (e.g., overall survival, progression-free survival, objective response rate), and associated statistical methodology (e.g., survival/time-to-event analysis, group sequential and adaptive designs).
  • Experience supporting regulatory submissions (e.g., NDA, BLA) is a strong plus.
  • Experience managing CROs and external statistical vendors, including oversight of outsourced statistical deliverables, is a plus.
  • Proficiency in statistical programming languages (e.g., SAS, R); experience using simulation to support trial design is a plus.
  • Knowledge of CDISC data standards (SDTM and ADaM).
  • Knowledge of drug submission requirements and relevant ICH and FDA/EMA guidelines, including the ICH E9(R1) estimand framework.
  • Strong verbal and written communication skills, including the ability to convey complex statistical concepts to cross-functional, non-statistical audiences.
  • Strong problem-solving skills and the ability to work both independently and collaboratively in a fast-paced environment.
  • Strong attention to detail and a proven ability to manage multiple competing priorities.

Washington State Pay Range - Associate Director: $200,850 - $227,316
Washington State Pay Range - Director: $235,000 - $263,700
Washington State Pay Range
$200,850-$263,700 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).

Apply