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Clinical Research Associate Intern Jobs (NOW HIRING)

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of ...

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How much do clinical research associate intern jobs pay per month?

As of Jul 15, 2026, the average monthly pay for clinical research associate intern in the United States is $6,439.50, according to ZipRecruiter salary data. Most workers in this role earn between $4,416.67 and $7,666.67 per month, depending on experience, location, and employer.

What does a Clinical Research Associate Intern do?

A Clinical Research Associate Intern assists in the monitoring and coordination of clinical trials to ensure they are conducted according to regulatory standards and study protocols. Interns may help with site visits, data collection, documentation, and communication between research teams and sponsors. This role provides hands-on experience in clinical research processes and helps interns develop an understanding of Good Clinical Practice (GCP) guidelines. Interns often work under the supervision of experienced clinical research professionals and gain valuable insight into the pharmaceutical or medical device industry.

What is the difference between Clinical Research Associate Intern vs Clinical Research Coordinator?

AspectClinical Research Associate InternClinical Research Coordinator
Required CredentialsTypically pursuing or holding a degree in life sciences; some internships require minimal certificationsUsually holds a bachelor's degree in health sciences or related field; certifications like CCRP are common
Work EnvironmentInternship setting within pharmaceutical companies or research institutions; supervised learningActive role in clinical trial sites; responsible for daily trial operations
Employer & Industry UsageUsed by pharmaceutical companies, CROs, and research institutions for trainingEmployed directly at clinical sites, hospitals, or research centers

While both roles involve clinical trial processes, a Clinical Research Associate Intern is primarily a learning position focusing on gaining experience, whereas a Clinical Research Coordinator manages the day-to-day operations of clinical trials at research sites.

What typical challenges do Clinical Research Associate Interns encounter when monitoring clinical trial sites?

Clinical Research Associate Interns often face challenges such as ensuring accurate data collection, maintaining regulatory compliance, and communicating effectively with site staff. Balancing these responsibilities while learning industry protocols can be demanding, especially when managing multiple sites or studies. Interns are supported by experienced team members, but must quickly adapt to varying site workflows and documentation standards to ensure trial integrity.

How much does a clinical research associate get paid?

A clinical research associate (CRA) typically earns between $50,000 and $85,000 annually, depending on experience, location, and the complexity of trials. Interns or entry-level CRAs usually start with lower salaries, often around $40,000 to $50,000 per year. Compensation can also include benefits such as health insurance and professional development opportunities.

What does a clinical research intern do?

A clinical research intern assists with the coordination and management of clinical trials by collecting data, preparing documentation, and ensuring compliance with study protocols. They often support senior staff with administrative tasks and may gain experience using research tools and software in a regulated environment.

Is 22 too old for an internship?

A Clinical Research Associate Intern position is typically open to candidates of various ages, including those who are 22. Age is generally not a barrier, and internships often value relevant skills, education, and enthusiasm over age, making 22 a suitable age for such opportunities.

What other jobs can a clinical research associate do?

A clinical research associate (CRA) can transition into roles such as clinical project manager, regulatory affairs specialist, or data manager, leveraging their knowledge of clinical trials, regulations, and data collection. They may also work in medical writing, quality assurance, or become study coordinators, often requiring additional certifications or experience in specific areas.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate Intern, and why are they important?

To thrive as a Clinical Research Associate Intern, you need a solid understanding of clinical trial protocols, regulatory guidelines (like GCP), and typically a background in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certifications like GCP training are highly valued. Strong attention to detail, organizational skills, and effective communication help interns excel in monitoring studies and collaborating with site staff. These skills are crucial for ensuring data integrity, regulatory compliance, and the smooth operation of clinical research projects.
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Clinical Research Associate Intern jobs near you
Clinical Research Associate I

Clinical Research Associate I

University of Nebraska Medical Center

Omaha, NE • On-site

$18.99 - $28.51/hr

Full-time

Posted 27 days ago

University Of Nebraska Medical Center rating

8.5

Company rating: 8.5 out of 10

Based on 15 frontline employees who took The Breakroom Quiz

52nd of 1,020 rated hospitals

Job description

GENERAL REQUISITION INFORMATION
EEO Statement:
UNMC is an Equal Employment Opportunity Employer, including an equal opportunity employer of protected veterans and individuals with disabilities.
Location Omaha, NE Requisition Number: Staff_14608 Department Int Med Rheumatology 50000594 Business Unit College of Medicine Reg-Temp Full-Time Regular Work Schedule As directed by supervisor Remote/Telecommuting No remote/telecommuting opportunity Position Summary
The Research Associate will play a crucial role in the successful execution and completion of research studies within the UNMC Division of Rheumatology. This position involves coordinating various aspects of research projects, including IRB submissions, participant recruitment, study visits, data collection, and timely submission of study data to sponsors. The ideal candidate will have a strong work-ethic, familiarity with clinical research methodologies, excellent organizational skills, and the ability to work collaboratively within a multidisciplinary team.
Position Details
Additional Information
Posting Category Research - Non Academic Working Title Clinical Research Associate I Job Title Clincal Research Associate L1 Salary Grade RA14H Appointment Type C2 - REG OFF/SERV HRLY Salary Range $18.990 - $28.510/hourly Job Requisition Begin Date 03/27/2026 Application Review Date 04/03/2026 Review Date Information:
Initial application review will begin on the date provided in the field above. Applications received prior to this review date will be considered. Applications received after the review date may be considered.
Required and Preferred Qualifications
Required Education: High School education or equivalent If any degree major/training is required, please specify the type. (NOTE: Concentration and minors are not equivalent to a major)
(Will consider three years related post high school education/experience)
Required Experience 3 years If any experience is required, please specify what kind of experience:
Experience related to healthcare, laboratory and/or clinical research
(Will consider three years related post high school education/experience)

Required License No If yes, what is the required licensure/certification? Required Computer Applications: Microsoft Excel, Microsoft Word, Microsoft Outlook Required Other Computer Applications: Required Additional Knowledge, Skills and Abilities:
Ability to work independently and as part of a team;
Ability to accurately follow study protocol guidelines;
Attention to detail in completing paperwork and data entry in a timely fashion;
Effective verbal and written communication skills; Effective organizational skills; Excellent verbal and written communication skills
Ability to identify potential problems.
Preferred Education: Relevant coursework/specialized training If any degree/training is preferred, please specify the type:
Training related to biological sciences, healthcare, laboratory and/or clinical research.
Preferred Experience: Preferred License: Yes If yes, what is the preferred licensure/certification?:
Phlebotomy certification, or willing to obtain.
Preferred Computer Applications: Preferred Other Computer Applications: Epic (Campus patient info system) Preferred Additional Knowledge, Skills and Abilities:
Have prior IRB and clinical research experience or be willing to be trained.
Email to a Friend https://unmc.peopleadmin.com/postings/97046

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