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Internship Clinical Trials Intern Jobs in Rochester, MN

LADC Internship

Rochester, MN

$14.75 - $19.50/hr

Plan and Goal Development- Interns will: • Develop a list of clinical goals based on 12 Core Functions and the intern's academic program expectations. • Review these goals with the MnTC intern ...

LADC Internship

Rochester, MN · On-site

$15.25 - $20.25/hr

Plan and Goal Development- Interns will: • Develop a list of clinical goals based on 12 Core Functions and the intern's academic program expectations. • Review these goals with the MnTC intern ...

The Echo Core Lab can accommodate clinical trials ranging in size from hundreds of studies to ... Interns sponsored by Mayo Clinic. Qualifications Must have a Ph.D., M.D., or equivalent doctoral ...

AI/ML Intern - Radiation Oncology

Rochester, MN · On-site

$15.25 - $19.75/hr

The Intern will interact with vast amounts of clinical and non-clinical data (external data sources, digital, etc.). Interns will learn the data science lifecycle including data acquisition ...

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Internship Clinical Trials Intern information

See Rochester, MN salary details

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How much do internship clinical trials intern jobs pay per hour?

As of Aug 30, 2026, the average hourly pay for internship clinical trials intern in Rochester, MN is $17.32, according to ZipRecruiter salary data. Most workers in this role earn between $14.66 and $19.57 per hour, depending on experience, location, and employer.

What does a clinical trials intern do?

An Internship Clinical Trials Intern assists with various aspects of clinical research studies, such as data collection, documentation, regulatory compliance, and participant communication. They work under the supervision of experienced clinical trial professionals to gain hands-on experience in the design, conduct, and monitoring of clinical trials. Typical responsibilities may include helping prepare study materials, entering data into databases, organizing trial documentation, and ensuring adherence to protocols and ethical standards.

What are the key skills and qualifications needed to thrive as a clinical trials intern?

To thrive as a Clinical Trials Intern, you generally need a background in life sciences or related fields, attention to detail, and familiarity with clinical research principles. Experience with data management systems like EDC, basic knowledge of regulatory guidelines such as GCP, and proficiency in Microsoft Office are typically required. Strong organizational skills, communication, and the ability to work collaboratively make a candidate stand out in this role. These skills are essential for ensuring accurate data collection, regulatory compliance, and effective teamwork in clinical research environments.

What types of projects or tasks are clinical trials interns typically assigned during their internship?

Clinical Trials Interns are often involved in a variety of supportive tasks that provide hands-on exposure to the clinical research process. Typical responsibilities may include assisting with data entry and management, supporting the preparation of regulatory documentation, coordinating with study sites, and helping monitor trial progress under supervision. Interns may also attend team meetings and collaborate with clinical research associates and project managers, gaining insight into the workflow of a clinical trials team. This experience offers a comprehensive view of the clinical research lifecycle and helps interns develop valuable skills for future roles in the industry.

What is the difference between Internship Clinical Trials Intern vs Clinical Research Coordinator?

AspectInternship Clinical Trials InternClinical Research Coordinator
Required CredentialsTypically pursuing or recent graduate in life sciences or related fieldBachelor's degree in health sciences, life sciences, or related field; certification often preferred
Work EnvironmentTemporary, educational setting, assisting with trial tasksFull-time, clinical setting managing ongoing trials
Employer & Industry UsageResearch institutions, pharmaceutical companies, universitiesHospitals, clinics, research organizations
Common Search & ComparisonYesYes

The Internship Clinical Trials Intern typically is a student or recent graduate gaining experience in clinical research, working under supervision. The Clinical Research Coordinator is a more experienced professional responsible for managing and coordinating clinical trials in a healthcare setting. While both roles involve clinical trial work, the intern role is more educational and entry-level, whereas the coordinator role requires more experience and responsibility.

What are popular job titles related to Internship Clinical Trials Intern jobs in Rochester, MN?

For Internship Clinical Trials Intern jobs in Rochester, MN, the most frequently searched job titles are:

What job categories do people searching Internship Clinical Trials Intern jobs in Rochester, MN look for?

The top searched job categories for Internship Clinical Trials Intern jobs in Rochester, MN are:

What cities near Rochester, MN are hiring for Internship Clinical Trials Intern jobs?

Cities near Rochester, MN with the most Internship Clinical Trials Intern job openings:

2025 Fall Intern, Clinical Applications

Rochester, MN


Zimmer Biomet
Medical Equipment and Supplies Manufacturing • 10K+ employees

7.7

Company rating: 7.7 out of 10

Based on 99 frontline employees who took The Breakroom Quiz

227th of 495 rated machine equipment manufacturers

People enjoy working here

Good employer

Recommended by students


$14.75 - $19.50/hr

Full-time

Re-posted 9 days ago


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


Zimmer Biomet logo

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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What Zimmer Biomet employees say

Pay

Benefits

Hours and flexibility

Workplace

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