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Clinical Trial Data Entry Jobs in Renton, WA (NOW HIRING)

YO AI Labs

Biostatistician Expert - Remote

Seattle, WA · Remote

$60 - $70/hr

Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs). * Produce and quality-check Tables, Figures & Listings (TFLs). * Review Clinical Study Reports ...

YO AI Labs

Biostatistician Expert - Remote

Seattle, WA · Remote

$60 - $70/hr

Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs). * Produce and quality-check Tables, Figures & Listings (TFLs). * Review Clinical Study Reports ...

SystImmune, Inc

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Familiarity with clinical trial data standards (CDISC SDTM, ADaM), experience with TLF generation preferred. * Experience integrating Spotfire with clinical databases and EDC systems (e.g., Medidata ...

Systimmune

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Familiarity with clinical trial data standards (CDISC SDTM, ADaM), experience with TLF generation preferred. * Experience integrating Spotfire with clinical databases and EDC systems (e.g., Medidata ...

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams ... Trial Managers, CRAs, Clinical Pharmacologists, Biomarker/Bioinformatics Scientists, Medical ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams ... Trial Managers, CRAs, Clinical Pharmacologists, Biomarker/Bioinformatics Scientists, Medical ...

YO AI Labs

Clinicia Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

In this role, you will help improve next-generation AI systems by evaluating clinical content, reviewing trial data, and providing expert medical judgment. No prior AI experience is required--your ...

New

YO AI Labs

Clinicia Expert - Remote

Seattle, WA · Remote

$150 - $200/hr

In this role, you will help improve next-generation AI systems by evaluating clinical content, reviewing trial data, and providing expert medical judgment. No prior AI experience is required--your ...

New

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All JobsClinical Trial Data Entry JobsClinical Trial Data Entry Jobs in Renton, WA

Clinical Trial Data Entry information

See Renton, WA salary details

$12

$42

$77

How much do clinical trial data entry jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for clinical trial data entry in Renton, WA is $42.37, according to ZipRecruiter salary data. Most workers in this role earn between $28.94 and $54.09 per hour, depending on experience, location, and employer.

What is a clinical trial data entry?

A Clinical Trial Data Entry job involves accurately inputting and managing clinical trial data in databases or electronic data capture (EDC) systems. Professionals in this role ensure that data from patient records, case report forms (CRFs), and research documents are entered correctly and comply with regulatory standards. They work closely with clinical researchers, data managers, and regulatory teams to maintain data integrity and confidentiality. Attention to detail, familiarity with medical terminology, and adherence to Good Clinical Practice (GCP) guidelines are essential for success in this role.

What are the key skills and qualifications needed to thrive in clinical trial data entry, and why are they important?

To thrive as a Clinical Trial Data Entry professional, strong attention to detail, data accuracy, and familiarity with medical terminology are typically required, often supported by a background in healthcare or life sciences. Proficiency with electronic data capture (EDC) systems, spreadsheets, and sometimes Good Clinical Practice (GCP) certification is valuable. Excellent organizational skills, time management, and the ability to collaborate within multidisciplinary research teams are key soft skills for success. These competencies ensure that clinical trial data is correctly entered, maintained, and integrated, which is crucial for regulatory compliance and the integrity of research outcomes.

What are the typical daily responsibilities of someone working in clinical trial data entry?

A Clinical Trial Data Entry professional is responsible for accurately entering and updating clinical trial data from source documents into electronic databases, verifying data for consistency, and flagging any discrepancies for resolution. The role often involves close collaboration with clinical research coordinators and other team members to ensure data completeness and compliance with study protocols. Additionally, they may help prepare reports, assist with database audits, and support data queries from regulatory authorities. This position requires strong attention to detail and adherence to strict timelines, as high-quality data is essential for the success of clinical trials.

What job categories do people searching Clinical Trial Data Entry jobs in Renton, WA look for?

The top searched job categories for Clinical Trial Data Entry jobs in Renton, WA are:

Clinical Trial Data Entry jobs near you
Infographic showing various Clinical Trial Data Entry job openings in Renton, WA as of August 2026, with employment types broken down into 91% Full Time, and 9% Temporary. Highlights an 90% In-person, and 10% Remote job distribution, with an average salary of $88,127 per year, or $42.4 per hour.

Senior / Principal Clinical Scientist, Clinical Development

Immunome, Inc.

Bothell, WA

Full-time

Posted 28 days ago

Job description

Position Overview

We are seeking a highly motivated and experienced Clinical Scientist to join our team. The Senior / Principal Clinical Scientist, Clinical Development will play a critical role in the design, execution, and interpretation of multiple clinical trials for our oncology drug candidates. This individual will work closely with cross-functional teams, including clinical operations, regulatory affairs, and research and development, to ensure the successful progression of multiple clinical programs. 

Responsibilities

  • Oversee the execution of clinical trials and ensure scientific and regulatory rigor. 
  • Design and develop multiple clinical trial protocols, informed consent forms, and other study-related documents. 
  • Collaborate with principal investigators, key opinion leaders, and clinical trial sites to ensure robust study design and execution. Serve as Lead Clinical Scientist for multiple trials. 
  • Conduct activities related to data generation and validation, including CRF design and clinical data review/query resolution. 
  • Contribute to the preparation of clinical study reports, regulatory submissions, and publications. 
  • Review development of site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (e.g., DMC) activities. 
  • Perform site-facing activities such as training and responding to clinical questions. 
  • Participate in the strategic development of clinical development plans and timelines. 
  • Present clinical trial data and findings to internal and external stakeholders, including scientific advisory boards and regulatory agencies. 
  • Mentor and develop junior team members with potential to manage direct reports. 

Qualifications

  • PhD, MD, PharmD, MS, or equivalent degree in life sciences. 
  • A minimum of 2 years of experience in clinical science, clinical research, or equivalent; clinical development experience is required, biopharmaceutical/biotechnology industry and oncology experience preferred. 
  • Strong leadership, project management, and communication skills. 
  • Travel may be required. 

Knowledge and Skills

  • Extensive experience in drug development process, study design, clinical operations. 
  • Extensive experience in clinical trial data analysis software and tools. 
  • Strong knowledge and skills to support program specific data review, trend identification, and data interpretation. 
  • Strong understanding of regulatory requirements and guidelines for clinical trials (e.g., GCP, ICH, FDA). 
  • Excellent analytical, organizational, and communication skills. 
  • Ability to work effectively in a fast-paced, collaborative environment. 
  • Strong problem-solving skills and attention to detail. 

WA State Range: Senior Clinical Scientist, Clinical Development - $145,823 - $182,019 

WA State Range: Principal Clinical Scientist, Clinical Development - $169,883 - $200,742 

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