Clinical Trial Management Intern

Clinical Trial Management Intern Late Phase

Join Us at Regeneron Pharmaceuticals Inc.

We are seeking a motivated and detail-oriented Clinical Trial Management Intern to join our dynamic team. This role is an exciting opportunity to immerse yourself in the world of clinical research supporting the execution of late-phase clinical trials. Youll work alongside experienced professionals gaining invaluable insights into clinical trial operations while contributing to impactful projects that drive innovation in healthcare.

As a valued team member youll collaborate with clinical study teams ensure compliance with regulatory standards and play a vital role in maintaining operational excellence. If youre passionate about clinical research and eager to learn this internship offers an incredible platform to grow and make a difference.

A Typical Day:
In this role youll engage in diverse responsibilities that provide a comprehensive view of clinical trial management. Your day may include:

• Coordinating and attending Clinical Study Team (CST) meetings preparing agendas materials and minutes.
• Supporting the organization of events such as investigator meetings and team sessions.
• Tracking site study start-up activities and maintaining study tools for progress monitoring.
• Assisting in the collection review and quality control (QC) of essential study documents and the electronic Trial Master File (eTMF).
• Collaborating with the eTMF lead to ensure study documentation is accurate complete and timely.
• Compiling and assembling study binders reference manuals and training materials under the guidance of clinical study leaders.
• Managing and updating team SharePoint or shared drive sites as needed.
• Participating in other CTM projects as assigned by the Senior Director of Clinical Trial Management.

This Role May Be For You If:
Youre a proactive and organized individual who thrives in a collaborative environment. You may excel in this role if:

• You enjoy working with global teams and communicating with diverse stakeholders.
• Youre detail-oriented and capable of juggling multiple tasks while maintaining accuracy.
• Youre comfortable using Microsoft Word Excel Outlook and PowerPoint.
• Youre eager to learn and contribute to a fast-paced clinical research environment.
• Youre confident in your ability to support administrative and operational aspects of clinical trials.
• Youre motivated to maintain high-quality standards in compliance with FDA regulations GCP and ICH guidelines.

To Be Considered:
To qualify for this internship you must:

• Be enrolled full-time in a Bachelors Masters or PhD program at an accredited university.
• Be continuing your studies full-time after completing the internship at Regeneron Pharmaceuticals Inc.
• Demonstrate excellent interpersonal collaboration and communication skills.
• Show a proactive self-motivated and organized approach to work.

This is your chance to contribute to meaningful clinical research while building a foundation for your future career. Join us at Regeneron Pharmaceuticals Inc. where innovation meets opportunity.

Does this sound like you Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits which vary by the U.S. benefits may include health and wellness programs (including medical dental vision life and disability insurance) fitness centers 401(k) company match family support benefits equity awards annual bonuses paid time off and paid leaves (e.g. military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US please visit For other countries specific benefits please speak to your recruiter.
Please be advised that at Regeneron we believe we are most successful and work best when we are together. For that reason many of Regenerons roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regenerons on-site policy and expectations for your role and your location.

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 nationality national or ethnic origin civil status age citizenship status membership of the Traveler community sexual orientation disability genetic information familial status marital or registered civil partnership status pregnancy or parental status gender identity gender reassignment military or veteran status or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment unless the accommodation would impose undue hardship on the operation of the Companys business.

For roles in which the hired candidate will be working in the U.S. the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S Japan or Canada please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity right to work educational qualifications etc.