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- Tasks: Join a global team to support drug development and regulatory strategies in oncology.
- Company: Be part of the world's leading healthcare company focused on innovative therapeutics.
- Benefits: Earn £18.80 per hour, gain hands-on experience, and receive mentorship.
- Why this job: Contribute to impactful projects while learning about cancer treatments and drug development processes.
- Qualifications: Must be an undergraduate student in relevant fields with strong communication and organizational skills.
- Other info: Opportunity to present your work at a research symposium and collaborate with diverse teams.
We have a fantastic opportunity to join the world’s most broadly-based healthcare company as a Regulatory Affairs Summer Intern. This is a full time (Monday to Friday – 37 hours) temporary role from May 12th – August 15th, 2025, based on their prestigious site in High Wycombe paying £18.80ph per hour.
Regulatory Affairs Summer Intern
2025 Summer Intern (Oncology TA) – (Undergraduate)
Job Description
As a summer intern, we offer an inclusive work culture that is open, innovative, and performance driven. As an intern you will be a member of a global matrixed team dedicated to the research and development of oncologic or immunologic therapeutics including execution of regulatory and clinical strategies covering complex compound programs in Phase I to III. The selected candidates will be assigned a mentor and will have the opportunity to contribute to projects in their function specific area. This role involves extensive global team matrix interactions with colleagues from several different disciplines. RA professionals are involved in all stages of the product lifecycle, and so can contribute to product development, registration with health authorities and management of medicinal products after marketing authorizations.
As an intern, you may contribute to Cross-Functional Trial Team (CFTT) activities and may also collaborate with other project teams in various functional disciplines supporting specific projects. The intern will have their own or group assigned projects and will be expected to present their work to their project teams, the oncology or immunology Senior Leadership Team (SLT), and as a poster/abstract at the research symposium at the end of the internship.
The goal of this internship program is to provide undergraduate students experience working in a large pharmaceutical R&D setting and to gain basic understanding of the science and process of novel drug development. Students will have the opportunity to learn aspects of cancer disease states, diagnosis, treatments, and the mechanism of action behind the emerging drugs being developed in our clinical trials. Students will also receive detailed training on Standard Operating Procedures (SOPs) as part of the Regulatory Scientist curriculum, trial specific training, and the clinical database software and medical data review tool.
Qualifications
Must be currently enrolled in an accredited University program throughout the duration of the internship
Undergraduate university students with completion of a minimum of three terms
Student in good standing, working towards the completion of an undergraduate degree
Must be currently enrolled in a biology, chemistry, clinical pharmacology/pharmacodynamics, pre-med, health sciences, public health, physician assistant, or nursing program or studies in Diversity, Equity, and Inclusion (DEI) or Health Equity/Disparities or similar areas
Must have a minimum cumulative passing grade point average reflective of all university coursework
Self-motivated and passionate about drug development and clinical research
Proven leadership/participation with campus programs and/or service programs is desired
Detailed oriented with good organizational skills
Possess strong leadership skills to participate and contribute to program initiatives and events
Fluent in written and spoken English
Great interpersonal, verbal and written communication skills
Good presentation skills; leading presentations to peers, project teams and senior leadership teams
Enthusiastic, collaborative, able to build relationships and work within global matrixed and cross-functional teams
Ability to work on and balance multiple project deliverables
Working knowledge and experience using key Microsoft suite of business tools including but not limited to Outlook, Excel, PowerPoint, Word, Teams, Slack, SharePoint, OneNote, etc.
Overall responsibilities may include:
Gaining overall understanding of clinical research and drug development including but not limited to Good Clinical Practices (GCPs), International Conference of Harmonization (ICH) guidelines, and Standard Operating Procedures (SOPs)
Participating in department and cross-functional team meetings
Shadowing key functional roles for learning/development opportunities
Collaboration and or assigned projects from other specific functional teams
Leadership opportunities on specific internship program activities and/or group projects
Abstract/poster preparation and presentation at organization-wide research symposium
Other projects assigned
Additional responsibilities as follows:
Conducting a research project on a topic impacting the regulatory function and business
Learning about regulatory strategy to support development of oncology products
Gaining exposure to preparation of clinical trial applications
Providing some support in product registration activities
Interacting with cross-functional team members involved in the development of novel therapies
Developing or enhancing communication, planning and organization skills in a diverse virtual team
Regulatory Affairs Summer Intern (Undergraduate) employer: ManpowerGroup
Contact Detail:
ManpowerGroup Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Summer Intern (Undergraduate)
✨Tip Number 1
Make sure to familiarize yourself with the latest trends and regulations in oncology and immunology. This knowledge will not only help you during the interview but also show your genuine interest in the field.
✨Tip Number 2
Network with professionals in the regulatory affairs space, especially those who work in oncology. Attend relevant webinars or workshops to connect with potential mentors who can provide insights into the role.
✨Tip Number 3
Prepare to discuss your previous experiences related to drug development or clinical research. Highlight any projects or coursework that demonstrate your understanding of Good Clinical Practices (GCPs) and regulatory guidelines.
✨Tip Number 4
Practice your presentation skills, as you will likely need to present your work to various teams. Being able to communicate your ideas clearly and confidently will set you apart from other candidates.
We think you need these skills to ace Regulatory Affairs Summer Intern (Undergraduate)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant coursework and experiences related to biology, chemistry, or clinical pharmacology. Emphasize any leadership roles or participation in campus programs that demonstrate your passion for drug development and clinical research.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the internship and how it aligns with your career goals. Mention specific skills you possess, such as strong communication and organizational skills, and how they will contribute to the team.
Showcase Relevant Skills: Highlight your proficiency in Microsoft Office tools and any experience with clinical research or regulatory affairs. If you have worked on group projects or presentations, be sure to mention these experiences to demonstrate your ability to collaborate effectively.
Proofread Your Application: Before submitting your application, carefully proofread all documents to ensure there are no spelling or grammatical errors. A polished application reflects your attention to detail and professionalism, which are crucial in the regulatory affairs field.
How to prepare for a job interview at ManpowerGroup
✨Show Your Passion for Drug Development
Make sure to express your enthusiasm for drug development and clinical research during the interview. Share any relevant experiences or projects that demonstrate your interest in oncology or immunology, as this will resonate well with the interviewers.
✨Highlight Your Teamwork Skills
Since this role involves extensive collaboration within a global matrixed team, be prepared to discuss examples of how you've successfully worked in teams. Emphasize your ability to build relationships and contribute to group projects.
✨Prepare for Technical Questions
Brush up on your knowledge of Good Clinical Practices (GCPs), International Conference of Harmonization (ICH) guidelines, and Standard Operating Procedures (SOPs). Being able to discuss these topics confidently will show your readiness for the internship.
✨Practice Your Presentation Skills
Since you'll be expected to present your work to various teams, practice your presentation skills ahead of time. Prepare a brief overview of a project or topic related to drug development that you can share during the interview to showcase your communication abilities.
