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Clinical Data Associate Internship 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 ...

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 ... equivalent internship or co-op experience in a clinical or pharma setting will be considered.

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 ... equivalent internship or co-op experience in a clinical or pharma setting will be considered.

Sumitomopharma

OR

$84.90K - $106.10K/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

$84.90K - $106.10K/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 ...

Lilly

OR

The Clinical Study Build Programmer will collaborate with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Manager and other key business partners to deliver ...

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Clinical Data Associate Internship information

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$86

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

As of May 29, 2026, the average hourly pay for clinical data associate internship 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 are the key skills and qualifications needed to thrive as a Clinical Data Associate Intern, and why are they important?

To thrive as a Clinical Data Associate Intern, you need attention to detail, analytical skills, and a background in life sciences or a related field. Familiarity with clinical data management systems (such as Medidata or Oracle Clinical) and knowledge of regulatory guidelines like GCP are typically required. Strong organizational, problem-solving, and communication skills set candidates apart in this role. These abilities ensure accurate data handling, regulatory compliance, and effective teamwork in clinical research projects.

What types of projects and tasks can I expect to work on during a Clinical Data Associate Internship?

As a Clinical Data Associate Intern, you will typically be involved in tasks such as data cleaning, verifying the accuracy of clinical trial data, and supporting database management activities. You may assist with data entry, help resolve discrepancies in clinical records, and work with clinical research teams to ensure data integrity. Interns often collaborate closely with data managers, statisticians, and clinical operations staff, gaining valuable exposure to the end-to-end process of clinical data handling. These experiences not only build technical and analytical skills but also provide insight into regulatory requirements and industry standards.

What is a Clinical Data Associate Internship?

A Clinical Data Associate Internship is a temporary position designed to provide hands-on experience in managing and analyzing data collected during clinical trials. Interns assist with tasks such as data entry, validation, quality control, and ensuring data integrity according to regulatory standards. This role is ideal for students or recent graduates interested in clinical research or data management in the healthcare industry. Interns typically work under the supervision of experienced clinical data associates and gain insights into the clinical trial process and regulatory compliance.

What is the difference between Clinical Data Associate Internship vs Clinical Data Associate?

AspectClinical Data Associate InternshipClinical Data Associate
CredentialsTypically pursuing or recent graduate in life sciences or related fieldBachelor's degree in life sciences, healthcare, or related field; some roles may require certification
Work EnvironmentInternship setting, often in pharmaceutical or biotech companies, with supervised tasksFull-time role in clinical research teams, handling data management independently
Employer & Industry UsageUsed as a training position in clinical research organizations and pharma companiesEstablished role in clinical trials and data management teams

The Clinical Data Associate Internship is a temporary training position designed for students or recent graduates to gain experience in clinical data management. In contrast, the Clinical Data Associate is a full-time professional role with greater responsibilities in managing clinical trial data independently. Both roles are essential in the clinical research industry, but the internship serves as a stepping stone toward a full-time career as a Clinical Data Associate.

More about Clinical Data Associate Internship jobs
What cities are hiring for Clinical Data Associate Internship jobs? Cities with the most Clinical Data Associate Internship job openings:
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Clinical Data Associate Internship jobs near you
Infographic showing various Clinical Data Associate Internship job openings in the United States as of May 2026, with employment types broken down into 1% Internship, 85% Full Time, and 14% Part Time. Highlights an 99% Physical, and 1% 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 20 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.

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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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