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Clinical Data Associate Internship Jobs (NOW HIRING)

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 · 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 ...

AbbVie

Associate, Data Sciences II

North Chicago, IL · On-site

Uses understanding of clinical trial concepts and cross-functional protocol requirements to execute ... academic, internships, or in a previous job) * Demonstrated effective communication skills

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role in ensuring the integrity, accuracy, and completeness of clinical trial data, contributing to the successful ...

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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 Jul 14, 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 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 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.

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 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.
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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 July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% 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.
Sr. Manager, Clinical Data Management

Sr. Manager, Clinical Data Management

Moderna, Inc.

Cambridge, MA • On-site

$130K - $209K/yr

Full-time

Medical, PTO

Posted 15 days ago

Moderna rating

8.9

Company rating: 8.9 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

7th of 74 rated pharmaceutical

Job description

The Role:
Moderna Services, Inc. seeks a Sr. Manager, Clinical Data Management for its Cambridge, Massachusetts location.
Here's What You'll Do:
  • Lead data management activities for in-house and outsourced studies.
  • Responsible for vendor oversight activities across global development programs.
  • Represent data management function in clinical cross-functional meetings, ensuring aligned expectations between the Contract Research Organization (CRO) and Moderna for all data related deliverables, especially in support of key decision points and regulatory submissions.
  • Ensure established milestones and deliverables are met with the highest degree of quality.
  • Partner with appropriate stakeholders and CRO partners to mitigate and resolve risks.
  • Provide input to functional governance with Moderna strategic suppliers.
  • Partner with appropriate stakeholders to resolve issues escalated from the vendor and/or cross-functional teams.
  • Lead and manage clinical trial data collection set-up, data review, and database lock for studies where data management activities are conducted within Moderna.
  • Work with other functions to complete set up of Electronic Data Capture (EDC) and study data collection tools such as Inter-response time (IRT), ePRO and eCOA.
  • Lead the creation and maintenance of study cross functional data review plan components, including edit checks (data validation plan), listing review checks, data integration specifications, data transfer specifications, external data reconciliation plans, coding guidelines, Serious Adverse Events (SAE) reconciliation guidelines, and database lock plans.
  • Lead data review, including query management, and activities required for interim and final database locks.
  • Ensure archival and inspection readiness of all Data Management Trial Master File (TMF) documents.
  • Ensure achievement of major data management deliverables and milestones in coordination with the Clinical Operations Clinical Development, Biostatistics & Programming, Biomarker Operations & Sample Management and Pharmacovigilance.
  • Plan and manage external Data Management budgets and timelines to ensure accuracy, understand trends in variances and support continuous improvement in forecasting.
  • Act as a process expert for operational and oversight models.
  • Maintain Standard Operating Procedures (SOPs), process maps and templates and timelines to support functions operational and oversight models.
  • May prepare metrics to support the function Key Performance Indicators (KPIs).
  • Represent function in external professional initiatives and organizations such as SCDM, CDISC, and DIA to identify industry best practice and increase the visibility of Moderna.
  • Lead functional Continuous Improvement initiatives, providing strategic direction and identifying key deliverables that meet timelines, budget, and are in alignment with requirements.
  • Work cross-functionally to ensure the quality of the data in each database and on time delivery, as well as quality of other data management deliverables.
  • Champion and adopt technology improvements and tools for use in clinical data management processes.
  • Ensure compliance with own Learning Curricula, corporate and GXP requirements.

Here's What You'll Bring to the Table:
Minimum requirements:
  • Requires a Bachelor's degree, or foreign equivalent, in Biotechnology, Biology, Biological Sciences, or related field and 8 years of progressive, post-baccalaureate experience as a Sr. Manager, Assistant Clinical Data Manager, Clinical Data Associate or related position supporting clinical data management for the pharmaceutical industry.
  • 7 years of experience must include:
    • Vendor Management;
    • Medidata RAVE, InForm, and Oracle Clinical EDC tools;
    • Clinical Data Management using Biomarker and External data;
    • Utilizing eTMF tools;
    • Study Database Lock processes including Final, Interim, Snapshots, DSUR submission, and Staggered Lock;
    • Study Initiation, CSR Review, and SAE Reporting;
    • J-Review, I-Review, and Clinbrowser; and
    • SDTM and CDISC datasets, Clinical Data Studio, SQL & SAS.
  • 100% telecommuting permitted from anywhere within the US.

The salary range for this role is $130,800 to $209,400. This range reflects the lowest to highest salary we, in good faith, believe we would pay for this role at the time of this posting. The minimum target pay for this particular position, based on its primary location, is $196,400 to $209,400. An individual's placement within the range will depend on several factors, including but not limited to specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs.
Apply at https://modernatx.wd1.myworkdayjobs.com/en-US/M_tx (Job ID: R19409) or email resume and cover letter to careers@modernatx.com with subject line: R19409.
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That's why our US benefits and global well-being resources are designed to support you-at work, at home, and everywhere in between.
  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investment opportunities to help you plan for the future
  • Location-specific perks and extras

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.
#dni
Pay & Benefits
At Moderna, we believe that when you feel your best, you can do your best work. That's why our benefits and well-being resources are designed to support you-at work, at home, and everywhere in between.
  • Competitive healthcare, plus voluntary benefit programs to support your unique needs
  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support
  • Family planning benefits, including fertility, adoption, and surrogacy support
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown
  • Savings and investments to help you plan for the future
  • Location-specific perks and extras

The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

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About Moderna

Sourced by ZipRecruiter

In just over a decade, Moderna has evolved from a research-focused company in the messenger RNA (mRNA) field to a leading enterprise with a diverse clinical portfolio of vaccines and therapeutics. With a strong intellectual property portfolio and state-of-the-art manufacturing capabilities, Moderna collaborates with global partners to advance groundbreaking science and achieve rapid scaling of production. Notably, Moderna's mRNA platform has enabled the development of therapies for various diseases, including infectious diseases, immuno-oncology, and cardiovascular conditions. Recognized as a top biopharmaceutical employer, Moderna fosters an inclusive and smoke-free work environment. The company is dedicated to equal employment opportunities and non-discrimination, ensuring that all employees and applicants are treated with respect and without bias based on factors like race, gender, religion, disability, or sexual orientation. Moderna is also committed to providing reasonable accommodations for individuals with disabilities, in accordance with applicable laws. To know more, visit www.modernatx.com.

Industry

Manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

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