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Clinical Data Associate Internship Jobs (NOW HIRING)

DCCC

Regional Data Associate

Washington, DC

$75K/yr

The Regional Data Associates will work with the Campaigns Data Director as well as the Organizing, Voter Protection, and Analytics teams to manage the flow of data between various data systems, voter ...

DCCC

Regional Data Associate

Washington, DC · On-site

$75K/yr

The Regional Data Associates will work with the Campaigns Data Director as well as the Organizing, Voter Protection, and Analytics teams to manage the flow of data between various data systems, voter ...

DCCC

Regional Data Associate

Washington, DC

$75K/yr

The Regional Data Associates will work with the Campaigns Data Director as well as the Organizing, Voter Protection, and Analytics teams to manage the flow of data between various data systems, voter ...

Biogen

Associate Director, Clinical Data Management

$167K - $230K/yr

The Associate Director of Clinical Data Management is a versatile and collaborative team member, influencing across functions and leadership to achieve program, operational, and organizational ...

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Clinical Data Associate Internship information

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$13

$38

$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:
What states have the most Clinical Data Associate Internship jobs? States with the most job openings for Clinical Data Associate Internship jobs include:
What job categories do people searching Clinical Data Associate Internship jobs look for? The top searched job categories for Clinical Data Associate Internship jobs are:
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.
eCOA - Clinical Study Build Programmer

eCOA - Clinical Study Build Programmer

Eli Lilly and Company

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 hours ago

Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 62 frontline employees who took The Breakroom Quiz

11th of 70 rated pharmaceutical

Job description

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.
The Clinical Study Build Programmer - eCOA is responsible for programming and testing clinical trial data collection databases, including the mapping, testing and normalization of data into a clinical data warehouse. This requires an in-depth understanding of data technology, data flow, data standards, database programming, normalization and testing. 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 standardized data collection methods and innovative validation solutions for use in global clinical trials.
Portfolio Delivery
  • Proficiency in programming and configuring clinical data collection systems (e.g., eCOA/EDC platforms)
  • Study build programming expertise (e.g., form logic, edit checks, workflows, integrations)
  • Program and test data collection systems and associated data repository mappings for a trial or set of trials within a program using data standards library components
  • Gather and influence eCOA design specifications and enable successful implementation
  • Understand study translation needs and enable localization
  • Ensure data collection systems and data warehouse mappings are delivered accurately, efficiently and in alignment with study objectives
  • Provide insights into the study design and data delivery (i.e. Data Management Plan, Project Plan, database, and observed datasets)
  • Support submission, inspection and regulatory response activities
  • Lead cross Business Unit/Therapeutic Area projects or programs with high complexity
  • Possess a deep understanding of the technology used to collect clinical trial data
  • Develops and tests new ideas and/or applies innovative solutions

Project Management
  • Increase speed, accuracy, and consistency in the development of systems solutions
  • Enable metrics reporting of study development timelines and pre and post production changes to database
  • Partner with Data and Analytics colleagues such as the Clinical Data Associate, Clinical Data Management Associate to deliver study database per business need and before first patient visit
  • Influence data standard decisions and strategies for a study and/or program
  • Effectively apply knowledge of applicable internal, external and regulatory requirements/expectations (MQA, CSQ, MHRA, FDA, ICH, GCP, PhRMA, Privacy knowledge, etc.) to study database building
  • Integrates multi-functional, external information and technical knowledge to support data-driven decision making

Enterprise Leadership
  • Continually seek and implement means of improving processes to reduce study build cycle time, decrease work effort and enable the normalization of various sources of data into a common data repository in a way that allows for improved integration, consumption and downstream analysis
  • Work to reduce postproduction changes change control process
  • Anticipate and resolve key technical, operational or business problems that impact the Data and Analytics organization
  • Thinks with end to end in mind consistently managing risk to minimize impact on delivery
  • Strong awareness with external developments, timelines
  • Focuses on defining database solutions and timelines in support of advancing the portfolio

Minimum Qualification Requirements:
  • Master's degree in a scientific field such as Informatics/Analytics, Life Sciences, Statistics, Information Technology, Epidemiology, Computer Sciences
  • + 3 years of related experience (or bachelor's degree plus 5 or more years of experience in clinical data management or areas that closely intersect with clinical data management e.g., statistics, data analytics, information technology, health outcomes, etc...)

Additional Preferences:
  • Experience with designing and handling eCOA data Articulating the flow of data (structure and format) from patient to analysis, applying this knowledge to data solutions
  • Deciding the technology platform (system/database) for data acquisition and aggregation Utilization of clinical/drug development knowledge and an ability to liaise with study team members (i.e. Data Sciences, Statistics, PK, Operations, Medical, etc.)
  • Strong therapeutic/scientific knowledge in the field of research Familiarity with clinical data tools and technologies
  • Understanding and experience in using data standards Ability to balance multiple activities, prioritize and manage ambiguity Domestic and International travel may be required

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$79,500 - $169,400
Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly

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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876

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