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Clinical Data Associate Ii Jobs (NOW HIRING)

Systimmune

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management activities across clinical trials, with a primary focus on Phase 3 and other large-scale studies. The ...

SystImmune, Inc

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management activities across clinical trials, with a primary focus on Phase 3 and other large-scale studies. The ...

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Clinical Data Associate Ii information

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How much do clinical data associate ii jobs pay per hour?

As of Jul 31, 2026, the average hourly pay for clinical data associate ii in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.

How does a Clinical Data Associate II typically collaborate with other teams during a clinical trial?

As a Clinical Data Associate II, you will work closely with clinical research coordinators, data managers, biostatisticians, and project managers to ensure the accuracy and integrity of clinical data. Collaboration often involves participating in cross-functional meetings, resolving data discrepancies, and supporting the database lock process. Effective communication and teamwork are essential, as you’ll coordinate data query resolutions and contribute to continuous process improvement with other departments. This collaborative environment provides opportunities to expand your knowledge in clinical research operations and build relationships that can support your career growth.

What is the salary of clinical data associate II in Thermo Fisher?

The salary for a Clinical Data Associate II at Thermo Fisher Scientific typically ranges from $60,000 to $80,000 per year, depending on experience, location, and education. This role often requires familiarity with clinical data management tools and adherence to regulatory standards.

What does a Clinical Data Associate II do?

A Clinical Data Associate II is responsible for managing and validating clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They review clinical data for completeness, identify discrepancies, and work with other clinical team members to resolve data issues. Their role often includes using specialized databases and software, performing quality checks, and generating reports to support clinical research studies. This position typically requires experience in clinical data management and knowledge of Good Clinical Practice (GCP) guidelines.

Is CRA an entry level job?

A Clinical Data Associate II (CDA II) is typically an intermediate role that requires prior experience or training in clinical data management. Entry-level positions in this field are usually labeled as Clinical Data Associate I or similar, with CDA II roles often requiring familiarity with electronic data capture systems and basic understanding of clinical trial processes.

What are the key skills and qualifications needed to thrive as a Clinical Data Associate II, and why are they important?

To thrive as a Clinical Data Associate II, you need a strong background in life sciences or related fields, experience in clinical data management, and a keen understanding of regulatory standards. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and often certifications like CDM or GCP are typically required. Attention to detail, problem-solving skills, and effective communication set outstanding professionals apart in this role. These skills are crucial to ensure data integrity, regulatory compliance, and successful clinical trial outcomes.

What does a clinical data associate do?

A clinical data associate is responsible for collecting, managing, and ensuring the accuracy of clinical trial data. They review data for completeness, resolve discrepancies, and use tools like electronic data capture (EDC) systems to support data quality and compliance with regulatory standards.

What is the difference between research associate 1 and 2?

In clinical data roles, a Research Associate I typically performs basic data entry and quality checks under supervision, while a Research Associate II handles more complex data management tasks, analyzes data, and may assist with protocol adherence. The II level usually requires more experience and may involve training or mentoring junior staff.
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Clinical Data Associate Ii jobs near you
Infographic showing various Clinical Data Associate Ii job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Clinical Data Associate - II

Integrated Resources INC

Foster City, CA

Contractor

Re-posted 13 days ago

Job description

Job Description

JOB DESCRIPTION:

  • Works collaboratively with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and other Clinical, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting.
  • Demonstrates a general understanding of each assigned protocol, critical tasks and milestones.
  • Ensure completeness, correctness and consistency of routine clinical data and data structure.
  • Assists in the implementation of routine clinical data management process with vendors including data entry, data quality checking, data transfer, reporting, backup, and recovery.
  • Assists in the preparation of CRF/eCRF for data collection through the regulatory approval process.
  • Assists in implementing routine clinical research projects. Reviews study protocol and assists site coordinators, investigators, and field clinical staff in collecting routine data to meet the protocol requirements in a timely manner.
  • Identifies, tracks, and resolves routine queries. Utilizes routine reports to track study progress and ensures timeliness and quality expectations are met.
  • Excellent verbal and written communication skills and interpersonal skills are required.
  • The ability to problem solve and have people/ project leadership skills.
  • Knowledge of FDA regulations, support of needs for NDA and other regulatory submissions, and familiarity with web-based Electronic Data Capture (EDC) and clinical data management systems.
Qualifications

Need to have 3-5 years of experience in data management( Pharma/ CRO/ Institute)

Additional Information

All your information will be kept confidential according to EEO guidelines.

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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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