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Clinical Trial Intern Jobs (NOW HIRING)

Zimmer Biomet

$14 - $18.75/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the ... Clinical Trial Management System (CTMS). How You'll Create Impact * Assist in testing and ...

Zimmer Biomet

$16 - $21.25/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the ... Clinical Trial Management System (CTMS). How You'll Create Impact * Assist in testing and ...

Zimmer Biomet

$14.75 - $19.75/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the ... Clinical Trial Management System (CTMS). How You'll Create Impact * Assist in testing and ...

Zimmer Biomet

$14.25 - $19.25/hr

What You Can Expect The Clinical Applications Intern is responsible for providing support to the ... Clinical Trial Management System (CTMS). How You'll Create Impact * Assist in testing and ...

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How much do clinical trial intern jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for clinical trial intern in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What does a clinical trial intern do?

A Clinical Trial Intern supports research teams in the planning, coordination, and execution of clinical studies. Their responsibilities often include assisting with data entry, maintaining study documentation, preparing study materials, and helping with regulatory compliance. Interns may also communicate with clinical sites, help track study progress, and ensure that protocols are followed. This experience provides valuable exposure to the clinical research process and helps interns develop skills relevant to a career in clinical trials.

What are some typical responsibilities of a clinical trial intern, and how do these tasks support the overall research process?

As a Clinical Trial Intern, you will often assist with data entry, documentation, and regulatory compliance tasks that are essential to the smooth running of clinical studies. Your responsibilities may include helping to prepare study materials, maintaining trial master files, and supporting communication between research teams and study sites. These tasks provide valuable hands-on experience in clinical research and directly contribute to ensuring that studies are conducted ethically and efficiently. Working closely with clinical coordinators and project managers, you'll gain insight into the end-to-end process of clinical trials, which can be a strong foundation for future roles in research or healthcare.

What are the key skills and qualifications needed to thrive as a clinical trial intern, and why are they important?

To thrive as a Clinical Trial Intern, you generally need a background in life sciences or a related field, attention to detail, and basic knowledge of clinical research processes. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and compliance with Good Clinical Practice (GCP) guidelines is often expected. Strong organizational skills, teamwork, and effective communication set standout interns apart in this role. These skills ensure accurate data handling, regulatory compliance, and smooth collaboration, which are crucial for the success of clinical trials.

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Clinical Trial Intern jobs near you

2025 Fall Intern, Clinical Applications

Zimmer Biomet

Montpelier, VT • On-site

$15.25 - $20.25/hr

Other

Re-posted 18 days ago

Zimmer Biomet rating

7.7

Company rating: 7.7 out of 10

Based on 99 frontline employees who took The Breakroom Quiz

230th of 499 rated machine equipment manufacturers

Job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.  

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards.  We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

The Clinical Applications Intern is responsible for providing support to the Biostatistics & Clinical Data Management (BCDM) department in the development and maintenance of software used in clinical research, primarily the Clinical Trial Management System (CTMS). 

How You'll Create Impact
  • Assist in testing and maintaining clinical software applications under the guidance of experienced developers and analysts.
  • Support the documentation of technical processes, user guides, and validation protocols.
  • Participate in requirements gathering sessions with stakeholders to better understand business and user needs.
  • Help monitor and track system issues, assisting in troubleshooting with supervision.
  • Perform basic data checks and assist with data validation efforts to ensure data integrity.
  • Observe and support user training sessions and help prepare training materials as needed.
What Makes You Stand Out
  • Strong written and verbal communication skills.
  • Ability to manage time effectively and handle multiple tasks or assignments under supervision.
  • Ability to work collaboratively as part of a team and communicate effectively with both technical and non-technical stakeholders.
  • Detail-oriented mindset with the ability to follow documented procedures and best practices.
  • Curiosity and willingness to learn about clinical applications and how technology supports clinical trials and research.
  • Proficiency in Microsoft Office tools, especially Excel, Word, and PowerPoint.
  • Exposure to or coursework in programming languages such as Java, JavaScript, SQL, Python, or similar.
  • Basic understanding of relational databases and familiarity with writing or reading simple SQL queries is a plus.
  • Interest in web development and knowledge of HTML and CSS, or UX/UI is a plus.
Your Background
  • Must be actively enrolled in an academic program for the entire duration of the assignment
  • Must be available to work full-time (40 hours/week) throughout the co-op session
  • Must be authorized to work in the U.S. without requiring employer sponsorship
  • Pursuing a bachelor’s degree in Computer Science, Information Systems, Health Informatics, Data Science, or related field.
  • A minimum GPA of 3.0 is strongly preferred
Travel Expectations
  • Up to 5%

EOE/M/F/Vet/Disability

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About Zimmer Biomet

Sourced by ZipRecruiter

Zimmer Biomet is a global medical technology leader. Our team members are part of a company with a heritage of leadership, a focus on shaping the future, and a mission dedicated to alleviating pain and improving the quality of life for people around the world.

Industry

Medical equipment and supplies manufacturing

Company size

10,000+ Employees

Headquarters location

Warsaw, IN, US

Year founded

1927

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