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Fda Intern Jobs in Hackensack, NJ (NOW HIRING)

Customs Compliance Intern (Fall 2026)

Newark, NJ · On-site

$41K - $50K/yr

Rename and file classification declarations, Food and Drug Agency (FDA) letters, and Other Government Agency / Partner Government Agency (OGA/PGA) declarations. Classification Database: * Assist with ...

Fda Intern information

See Hackensack, NJ salary details

$9

$18

$26

How much do fda intern jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for fda intern in Hackensack, NJ is $18.58, according to ZipRecruiter salary data. Most workers in this role earn between $15.72 and $20.96 per hour, depending on experience, location, and employer.

What is the difference between Fda Intern vs Fda Associate?

AspectFda InternFda Associate
Required CredentialsTypically pursuing or holding a relevant degree (e.g., life sciences, pharmacy)Bachelor's or master's degree in a related field, with some roles requiring additional certifications
Work EnvironmentInternship programs within FDA offices, often temporary and training-focusedFull-time employment in FDA regulatory or compliance departments
Employer & Industry UsageUsed mainly for entry-level training positions during educationUsed for professional roles with increased responsibilities in regulatory affairs

The main difference between an Fda Intern and an Fda Associate is the level of experience and responsibility. Interns are typically students gaining exposure, while Associates are full-time employees handling more complex tasks within FDA operations.

What types of projects and responsibilities can an FDA intern expect during their internship?

As an FDA Intern, you can expect to work on a variety of projects that support public health initiatives, regulatory research, and policy analysis. Typical responsibilities may include data collection and analysis, assisting with the review of regulatory documents, participating in team meetings, and supporting outreach or educational programs. Interns often collaborate with experienced scientists, policy analysts, and regulatory specialists, gaining hands-on exposure to the federal regulatory process. The environment is collaborative and fast-paced, providing valuable experience and insight into the workings of a major government agency.

What does an FDA intern do?

An FDA intern typically assists with various tasks related to the regulation and oversight of food, drugs, medical devices, and other products overseen by the U.S. Food and Drug Administration. Their responsibilities may include supporting research projects, analyzing data, preparing reports, and helping with administrative duties. Interns gain valuable experience in public health, regulatory policy, and scientific research, working alongside experienced professionals. The specific duties can vary depending on the department and the intern’s educational background.

What are the key skills and qualifications needed to thrive as an FDA intern?

To thrive as an FDA Intern, you generally need a background in life sciences, public health, or a related field, often supported by enrollment in or completion of a relevant degree program. Familiarity with regulatory databases, Microsoft Office Suite, and possibly data analysis tools like SAS or Excel is beneficial. Strong analytical thinking, attention to detail, and effective communication skills help interns contribute meaningfully and collaborate with regulatory professionals. These skills are crucial for ensuring compliance with regulations, supporting public health initiatives, and gaining valuable experience in a highly regulated environment.
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What cities near Hackensack, NJ are hiring for Fda Intern jobs? Cities near Hackensack, NJ with the most Fda Intern job openings:
Infographic showing various Fda Intern job openings in Hackensack, NJ as of August 2026, with employment types broken down into 17% Internship, 1% As Needed, 52% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $38,648 per year, or $18.6 per hour.

Summer 2026 MD Intern, Internal Medicine

Regeneron Pharmaceuticals

Tarrytown, NY • On-site

$32 - $40.70/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 22 days ago


Regeneron rating

8.7

Company rating: 8.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical


Job description

If you're currently a medical school student interested in drug discovery and development, you may be a fit for an internship in our Internal Medicine Clinical Development Unit.

In this role, a typical internship will include:

  • Achieving a general understanding of what happens in our global development organization

  • Completing a hands-on project that has an impact on the business

  • Engaging with Regeneron leadership

  • Collaborating with a specific hiring manager and other interns

  • Establishing connections with Regeneron's diverse employee resource groups

  • Participating in professional development sessions

  • Showcasing the knowledge you gained through end of program presentation sessions

  • Getting paid for your hard work!

Internship Project Specifics:

The summer intern will be placed on a project team in the Internal Medicine Clinical Development Unit at Regeneron. During this project the summer intern may visually and/or descriptively analyze clinical trial data from recent studies or databases. Disease areas that comprise the focus of the summer interns project may include: cardiovascular, pulmonary and/or immunological & inflammatory diseases.

The student will be trained on basic statistical modeling techniques using SAS JMP. The summer project may involve reviewing pharmacokinetic (PK) and pharmacodynamic (PD) data from clinical trials. Students will be trained on techniques for data cleaning, statistical analysis, and linear regression (univariate and multivariate). The student will work closely with the global program head, medical director and clinical pharmacology director during the project.

Additionally, students will be trained in Good Clinical Practice (GCP) standards for human clinical trials including relevant International Conference on Harmonization (ICH) and FDA Guidelines. The student will also attend relevant team meetings including: Strategic Project Team, Global Clinical Sub Team, Global Regulatory Sub Team and others as needed.

At the end of the summer internship period, the student will be expected to give a presentation/summary of their research experiences to an internal audience at Regeneron.

To be considered for this opportunity, you must be currently enrolled in medical school and returning to school the semester following the internship). A cumulative GPA of 3.0 is preferred. We want someone who is able to commit to 40 hours per week for a minimum of 6-8 weeks during a time-period from the end of May/ early June through August. The specific weeks of the internship are flexible and intended to accommodate the intern's time out of school. Demonstrated leadership in areas such as campus activities, clubs, sports, current or previous work, or within the community is also preferred.

Requirements:

  • Medical student currently enrolled in an accredited US medical school (MD)

  • Must have completed at least the first-year basic science curriculum. Students who have completed the second year and beyond will also be considered but must have adequate time available during an elective or research rotation to be on site at Regeneron.

  • Familiarity with Microsoft Office tools (Word, Outlook, Powerpoint).

  • Prior research experience is preferred but not required. Understanding of biostatistics, experimental design and the scientific method is preferred. Experience with R studio, Python, SPSS, SAS or SAS JMP is a plus.

  • On site attendance at Regeneron offices in Tarrytown NY is expected 5 days per week

Please note our intern pay ranges are determined by level of education (year in school) and degree program. The hourly rate range for Tarrytown, NY: $32.00-$40.70 per hour.


Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.


Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.


As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.


For jobs in Canada: this posting is for an existing position.


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