Looking for clinical research internships or regulatory affairs internships in the USA? Advarra is offering a paid Regulatory Intern position for Summer 2026. This full-time or part-time remote internship is perfect for undergraduate or graduate students pursuing degrees in business, law, or biomedical research. Applications are open for the cohort running from June 1 to August 7, 2026.
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About the Company
Advarra is a market leader and pioneer in clinical research solutions, providing Institutional Review Board (IRB), Institutional Biosafety Committee (IBC), and advanced technology services. The company helps align patients, research sites, sponsors, and CROs to accelerate clinical trials while maintaining the highest standards of ethics, quality, and compliance.
With a strong focus on innovation and patient-centricity, Advarra supports the advancement of human health through ethical review services and cutting-edge technology. The company fosters an inclusive, collaborative culture where employees are empowered to make a meaningful impact.
Job Details
- Company Name: Advarra
- Job Title: Regulatory Intern
- Job Category: IRB Operations
- Requisition Number: REGUL004340
- Location: Remote (United States)
- Job Type: Full-time or Part-time Internship
- Duration: June 1, 2026 – August 7, 2026
- Hourly Pay: $22 per hour
- Posted Date: April 9, 2026
Job Description
Advarra’s Summer Intern Program offers an enriching experience for students to gain practical exposure in regulatory compliance within the Human Research Protection Program (HRPP).
The Regulatory Intern will support the Regulatory Compliance department in managing IRB reliance agreements, IBC registrations, and various administrative and project-related tasks.
Interns will work closely with the Regulatory team and have opportunities to network with senior leaders across the organization.
Key Job Duties & Responsibilities
- Perform administrative tasks for tracking, storage, and maintenance of IRB reliance agreements and IBC registrations
- Support the use of Research Services Zendesk and assist with report creation in Explore
- Contribute to assigned regulatory projects, including the development of the Advarra Help Knowledge Center
- Collaborate with Regulatory Department members on HRPP-related responsibilities
- Provide support to internal and external stakeholders including IRB/IBC teams, sites, sponsors, and research participants
Skills/Qualifications
Basic Qualifications
- High school diploma required
- Currently enrolled as an undergraduate or graduate student pursuing a degree in business, law, or biomedical research studies (preferred)
- Available to work between 9:00 AM – 5:00 PM EST from June 1 to August 7, 2026
- Must be currently authorized to work in the United States
Preferred Qualifications
- Strong problem-solving skills and personal integrity
- Excellent communication, organizational, and attention-to-detail skills
- Ability to prioritize and manage multiple tasks
- Proficiency in Microsoft Office (Word, Excel, Outlook, SharePoint)
- Experience with data entry
- Familiarity with Customer Relationship Management (CRM) software such as Zendesk (preferred)
Key Responsibilities
- Track and maintain regulatory documents and agreements
- Assist with Zendesk ticket management and reporting
- Support ongoing regulatory projects and knowledge base development
- Collaborate effectively with team members on compliance tasks
- Ensure accuracy and attention to detail in all administrative work
Benefits/Perks
- Competitive hourly pay of $22/hr
- Valuable hands-on experience in clinical research regulatory affairs
- Networking opportunities with senior leaders and fellow interns
- Exposure to IRB, IBC, and Human Research Protection Program operations
- Fully remote work arrangement
- Supportive and inclusive company culture focused on learning and growth
How to Apply
Apply directly for Requisition Number: REGUL004340 through the official Advarra Careers portal.
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Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Advarra Career page.
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For more clinical research internships, regulatory internships, pharma internships, and healthcare opportunities in the USA and India, visit Pharma Recruiter.
Don’t miss this summer 2026 internship opportunity — apply early!
Why You Should Join Advarra
Advarra’s Regulatory Intern program provides a meaningful entry point into the world of clinical research ethics and regulatory compliance. You will gain practical skills, contribute to important HRPP functions, and work in a purpose-driven organization that values innovation, ethics, and patient safety.
This internship is an excellent stepping stone for students aspiring to build a career in clinical research, regulatory affairs, or life sciences.
FAQs
What is the duration of the Advarra Regulatory Intern program?
The internship runs from Monday, June 1, 2026, to Friday, August 7, 2026.
Is this a paid internship?
Yes, the position offers competitive pay at $22 per hour.
Is the Regulatory Intern role fully remote?
Yes, the role is 100% remote within the United States.
Who is eligible to apply for this internship?
Undergraduate or graduate students (or recent high school graduates planning to pursue higher education) with interest in business, law, or biomedical research are encouraged to apply.
What skills are most important for success in this role?
Strong attention to detail, organizational skills, proficiency in Microsoft Office, and excellent communication abilities are highly valued.
Would like to work part time from Remote area