Global Trial Optimisation Intern

At Regeneron, we are dedicated to improving lives through science. As a Global Trial Optimisation (GTO) Intern, you will play a vital role in shaping clinical trial feasibility and patient recruitment strategies, contributing to the success of global clinical development programs. This internship offers an exciting opportunity to gain hands-on experience in a dynamic research environment while supporting data-driven decision-making that impacts the future of healthcare. Join us in advancing clinical trial innovation while developing your skills in data analysis, operational planning, and process improvement.

A Typical Day:
As a GTO Intern, your day may include:

Collaborating with the GTO Specialist to identify, generate, and analyze clinical trial data.Supporting feasibility and recruitment strategies to enhance study protocols and operational plans.Managing investigator site and healthcare provider-level data for resource planning and vendor oversight.Contributing to process improvement initiatives and monitoring compliance with policies and best practices.Learning and applying principles of ICH Good Clinical Practice (GCP) in a regulated industry.Utilizing clinical trial systems such as CTMS, ODR, EDC, and other reporting tools.Partnering with external data providers and analytics teams to optimize trial operations.Assisting in patient engagement planning and supporting diversity, equity, and inclusion strategies in clinical trials.

This Role May Be For You If:
You are someone who:

Thrives on analyzing and interpreting data to drive impactful decisions.Enjoys collaborating with cross-functional teams in a fast-paced, scientific environment.Is eager to learn about clinical trial management systems and operational tools.Values attention to detail and compliance with industry standards.Is passionate about improving patient recruitment and engagement strategies.Has a proactive approach to process improvement and change management.Appreciates the opportunity to gain exposure to clinical operations and drug development processes.Is motivated by contributing to meaningful advancements in healthcare.

To Be Considered:
Candidates must have a strong interest in clinical research and data analytics. Required qualifications include familiarity with data analysis tools and systems, as well as a foundational understanding of clinical trial processes. Preferred qualifications include experience with clinical trial management systems, operational data repositories, and electronic data capture tools. Prior exposure to regulated environments or GCP principles is a plus.

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 location.  In 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 https://careers.regeneron.com/en/working-at-regeneron/total-rewards/.  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 Regeneron’s roles are required to be performed on-site. Please speak with your recruiter and hiring manager for more information about Regeneron’s 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 Company's 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.