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Clinical Data Associate Per Diem Jobs (NOW HIRING)

Lilly

Clinical Data Associate

Indianapolis, IN

The Clinical Data Associate is accountable for the end-to-end clinical data sciences delivery for a clinical study, including clinical database build, data acquisition, storage, retrieval, and ...

NYULMC

Research Data Associate- Per Diem

New York, NY · On-site

$29.56/hr

We have an exciting opportunity to join our team as a Research Data Associate- Per Diem. This is an ... This position will provide assistance to the research team for various aspects of clinical research.

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 ... Perform UAT (User Acceptance Testing) of EDC systems and edit checks per provided specifications ...

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 ... Perform UAT (User Acceptance Testing) of EDC systems and edit checks per provided specifications ...

Sumitomopharma

OR · On-site

$84K - $106K/yr

The Senior Clinical Data Associate (Sr. CDA) works in close partnership with Lead/Clinical Data Managers (LDM/CDM) and supports multiple oncology studies with increased independence and ...

Sumitomo Pharma

Senior Clinical Data Associate

$84K - $106K/yr

The Senior Clinical Data Associate (Sr. CDA) works in close partnership with Lead/Clinical Data Managers (LDM/CDM) and supports multiple oncology studies with increased independence and ...

NYULMC

Per Diem Research Data Associate

New York, NY · On-site

The Research Data Associate (RDA) will work per diem to contribute to clinical research efforts within the Schizophrenia Research Group at the Department of Psychiatry, NYU Langone Health. Under the ...

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Clinical Data Associate Per Diem information

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

As of Jun 11, 2026, the average hourly pay for clinical data associate per diem 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.

What is the difference between Clinical Data Associate Per Diem vs Clinical Data Coordinator?

AspectClinical Data Associate Per DiemClinical Data Coordinator
CertificationsTypically requires a degree in life sciences or related field; certifications like CDISC or CDMP are a plusSimilar certification requirements; often holds additional project management or data management certifications
Work EnvironmentTemporary, flexible schedules; often in clinical research settingsFull-time, permanent roles; involved in ongoing data management projects
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for short-term data tasksEmployed by similar organizations for overseeing data integrity and compliance

The main difference is that Clinical Data Associate Per Diem roles are temporary and flexible, focusing on specific data tasks, while Clinical Data Coordinators hold permanent positions with broader responsibilities in managing clinical data processes.

More about Clinical Data Associate Per Diem jobs
What cities are hiring for Clinical Data Associate Per Diem jobs? Cities with the most Clinical Data Associate Per Diem job openings:
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Clinical Data Associate Per Diem jobs near you
Infographic showing various Clinical Data Associate Per Diem job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 91% Full Time, 2% Part Time, and 5% 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

Clinical Data Associate

Integrated Resources INC

Foster City, CA • On-site

Contractor

Posted 3 days ago

Job description

Job Description

1) Lead clinical data manager with 3 -5 years of Sponsor or CRO or Academic experience

2) Project management experience of clinical trials

3) Understanding of clinical data management processes

4) Communication with cross-functional study team members

Specific Responsibilities:

  • This role will immediately assume biomarker data management responsibilities for representing biomarker data management at the biomarker Sub Team (BST) meetings. The candidate will also be responsible for providing oversight to studies that fall within the BSTs.
  • The selected candidate will manage biomarker data in various stages, from planning, to set-up, conduct, closeout, and archiving, in high volume, while maintaining a high level of data quality by leveraging and adhering to standard data structures and corresponding standard edit checks and review listings.
  • The selected candidate may also manage and lead in the design and implementation of biomarker data management processes with vendors, ensuring completeness, correctness, and consistency according to the Client's standards.
  • This role has a high degree of collaboration with the Biomarker cross-functional team members, study team members and other biomarker Clinical Data Associates.

The ideal candidate should possess a BS degree or higher in a Biomedical Science or equivalent and minimum 3 years of relevant clinical data management experience and preferably along with biomarker or laboratory background and experience in a CRO or bio/pharmaceutical setting.

  • Essential Duties and Job Functions:
  • Works collaboratively with Biomarker Clinical Operations team members, Biomarker Scientists, Biomarker Statistical Programming group, Biomarker Biostatistics group, Biomarker Clinical Programming group, Biobanking and Sample Management group, and lead study clinical data associate and cross-functional study team members to meet project deliverables and timelines for biomarker 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.
  • Responsibilities include: assisting in the developing the data transfer specifications, the data mapping specifications, the data quality review plan and the data validation specifications, vendor management, data review and data reconciliation. Assists in implementing routine clinical research projects and standards.
  • Identifies, tracks, and resolves routine queries. Utilizes routine reports to track study progress and ensures timeliness and quality expectations are met.
  • Knowledge, Experience and Skills: 3 years of experience and a BS degree.
  • 1 years of experience and a MS degree or PhD.
Additional Information

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

Integrated Resources logo

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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