At a Glance
- Tasks: Support safety monitoring of medicines in clinical trials and contribute to impactful projects.
- Company: Join a leading biopharmaceutical company dedicated to patient safety.
- Benefits: Comprehensive benefits, including health programs, fitness centres, and paid time off.
- Why this job: Gain hands-on experience in drug safety while making a difference for patients worldwide.
- Qualifications: Pursuing or recently completed a degree in life sciences; strong writing and communication skills.
- Other info: Collaborative environment with opportunities for growth and learning.
The predicted salary is between 500 - 1500 £ per month.
We are seeking a passionate and detail-oriented Global Patient Safety Intern to support our team in monitoring the safety of medicines in clinical trials and marketed products. This role offers a unique opportunity to gain foundational training in drug safety and pharmacovigilance while contributing to meaningful work that impacts patients globally. As part of our team, you'll work alongside experienced safety leads and scientists, gaining hands-on experience in safety surveillance activities for our portfolio of medicines. If you're looking for a role that combines learning, collaboration, and real-world impact, this is your chance to make a difference.
A Typical Day:
- Participate in signal management activities by retrieving and reviewing safety data and preparing signal evaluation reports.
- Assist with the preparation of risk management plans and draft responses to regulatory inquiries.
- Contribute to the preparation of periodic safety reports for medicines in clinical development and marketed products.
- Organize, support, and actively participate in Safety Management Team (SMT) meetings.
- Collaborate with cross-functional teams, including clinical study, regulatory, and case processing teams, to complete Safety Sciences activities.
This Role May Be For You If:
- You are currently pursuing or have recently completed a degree in life sciences.
- You are eager to learn about clinical trials and regulatory processes (prior knowledge is a plus but not required).
- You excel in technical writing and oral communication.
- You thrive in collaborative environments and enjoy working in cross-functional teams.
- You have a keen eye for detail and can meet deadlines with precision.
To Be Considered:
- You must be currently enrolled in or have recently completed a degree in life sciences.
- While prior knowledge of clinical trial processes is advantageous, it is not essential.
- Strong technical writing and communication skills are crucial, along with the ability to work effectively in cross-functional teams and adhere to deadlines.
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.
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.
GPS Safety Sciences Intern employer: Regeneron Pharmaceuticals
Contact Detail:
Regeneron Pharmaceuticals Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land GPS Safety Sciences Intern
✨Tip Number 1
Network like a pro! Reach out to your connections in the life sciences field and let them know you're on the hunt for an internship. You never know who might have a lead or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical trials and pharmacovigilance. We recommend practising common interview questions with a friend or even in front of the mirror to boost your confidence.
✨Tip Number 3
Show off your communication skills! During interviews, be sure to articulate your thoughts clearly and concisely. Remember, they want to see how well you can convey complex information, so don’t hold back!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining our team and making a difference in patient safety.
We think you need these skills to ace GPS Safety Sciences Intern
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Global Patient Safety Intern role. Highlight your relevant skills and experiences that align with the job description, especially your technical writing and communication abilities.
Show Your Passion: Let your enthusiasm for drug safety and pharmacovigilance shine through in your application. We want to see your eagerness to learn and contribute to meaningful work that impacts patients globally.
Be Detail-Oriented: Pay close attention to detail when filling out your application. Double-check for any typos or errors, as precision is key in this field. A polished application reflects your commitment to quality.
Apply Through Our Website: We encourage you to apply directly through our website. This ensures your application gets to the right people and shows that you're serious about joining our team at Regeneron.
How to prepare for a job interview at Regeneron Pharmaceuticals
✨Know Your Stuff
Before the interview, brush up on your knowledge of drug safety and pharmacovigilance. Familiarise yourself with key terms and concepts related to clinical trials and safety data. This will not only show your enthusiasm but also help you engage in meaningful discussions during the interview.
✨Showcase Your Skills
Highlight your technical writing and communication skills by preparing examples of your work. Whether it's a report or a presentation, be ready to discuss how you approached these tasks and what you learned from them. This will demonstrate your ability to contribute effectively to cross-functional teams.
✨Ask Smart Questions
Prepare thoughtful questions about the role and the company. Inquire about the Safety Management Team's processes or how they handle regulatory inquiries. This shows that you're genuinely interested in the position and eager to learn more about their operations.
✨Be Collaborative
Emphasise your experience working in teams. Share examples of how you've successfully collaborated with others in past projects. This is crucial for a role that thrives on teamwork, and it will reassure the interviewers that you can fit into their collaborative culture.