About the Company
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to pushing the boundaries of human health by harnessing data science and human expertise to help our clients develop innovative medicines faster and more efficiently. Join our team in Oxford, a hub of scientific innovation, and contribute to meaningful work that impacts patients worldwide.
Job Description
We are seeking a highly motivated and detail-oriented Food & Drug Administration (FDA) Compliance Intern to join our team in Oxford. This entry-level internship offers a unique opportunity to gain practical experience in regulatory affairs and compliance within the pharmaceutical and healthcare sectors. The intern will support our compliance specialists in ensuring adherence to FDA regulations, internal policies, and industry best practices. This role is ideal for students or recent graduates interested in a career in regulatory compliance, quality assurance, or life sciences. Full training will be provided, making this an excellent opportunity for individuals with little to no prior professional experience in the field.
Key Responsibilities
- Assist in the review and organization of regulatory documents, ensuring accuracy and completeness.
- Support the preparation of compliance reports and presentations.
- Research and summarize current FDA regulations, guidance documents, and industry standards.
- Collaborate with compliance specialists on ongoing projects related to quality management systems and regulatory submissions.
- Help maintain compliance databases and tracking systems.
- Participate in internal training sessions and team meetings.
- Contribute to the development and improvement of compliance processes and procedures.
- Provide administrative support to the compliance team as needed.
Required Skills
- Currently enrolled in or a recent graduate of a Bachelor's or Master's degree program in Life Sciences, Pharmacy, Regulatory Affairs, Law, or a related field.
- Strong interest in regulatory compliance, particularly FDA regulations.
- Excellent written and verbal communication skills.
- High level of attention to detail and organizational abilities.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
- Ability to work effectively both independently and as part of a team.
- Eagerness to learn and adapt in a fast-paced professional environment.
Preferred Qualifications
- Familiarity with basic principles of Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), or Good Laboratory Practice (GLP).
- Prior academic exposure to regulatory affairs or quality assurance concepts.
Perks & Benefits
- Competitive hourly pay.
- Opportunity to work with industry experts in a global company.
- Structured mentorship and professional development opportunities.
- Exposure to real-world FDA compliance challenges.
- Networking opportunities within the life sciences industry.
- Access to company learning resources and internal training programs.
- Modern office environment in a vibrant academic city.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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