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- Tasks: Join us as a Regulatory Affairs Associate, handling licensing and regulatory procedures.
- Company: Work with one of the largest pharmaceutical companies tackling urgent medical needs.
- Benefits: Enjoy a competitive hourly rate and the chance to work in a dynamic environment.
- Why this job: Make a real impact in healthcare while developing your skills in a supportive team.
- Qualifications: A relevant scientific degree and basic knowledge of the regulatory landscape are essential.
- Other info: This is a 12-month contract role based in Basingstoke; DBS check required.
CK Group are recruiting for a Regulatory Affairs Associate, to join a company in the pharmaceutical industry, at their site based in Basingstoke, on a contract basis for 12 months.
Salary: PAYE £14.68 - £19.37 per hour.
Regulatory Affairs Role:
- License maintenance activities (e.g. Labelling changes, CMC changes, Renewals).
- New marketing authorisations, line extensions and new indications.
- Tracking regulatory procedures and filing/archiving correspondence in accordance with local regulations and quality system requirements.
- Provide operational excellence to successfully achieve affiliate regulatory objectives.
- Facilitate and cultivate relationships with relevant external regulatory personnel.
Your Background:
- Bachelor's degree or equivalent in a relevant scientific subject.
- Foundational knowledge and understanding of regulatory environment.
- Good communication skills and the ability to prioritise different tasks.
- Demonstrated good computer/IT skills.
- Team working skills with special focus on results.
Company: Our client is one of the largest pharmaceutical companies in the world. They focus on finding answers for some of the world's most urgent medical needs.
Location: This role is based at our client's site in Basingstoke.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference in all correspondence.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
If this position isn't suitable but you are looking for a new role, or if you are interested in seeing what opportunities are out there, head over to our LinkedIn page (cka-group) and follow us to see our latest jobs and company news.
Regulatory Associate employer: CK Group- Science, Clinical and Technical
Contact Detail:
CK Group- Science, Clinical and Technical Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Associate
✨Tip Number 1
Familiarise yourself with the specific regulatory requirements in the pharmaceutical industry. Understanding local regulations and quality system requirements will give you an edge during interviews, as you'll be able to demonstrate your knowledge and readiness for the role.
✨Tip Number 2
Network with professionals already working in regulatory affairs. Attend industry events or join relevant online forums to connect with others in the field. This can provide valuable insights and potentially lead to referrals for the position.
✨Tip Number 3
Highlight your communication skills during any discussions or interviews. Since the role involves cultivating relationships with external regulatory personnel, showcasing your ability to communicate effectively will be crucial in making a strong impression.
✨Tip Number 4
Prepare to discuss your experience with license maintenance activities and any relevant projects you've worked on. Being able to share specific examples of how you've handled similar tasks will demonstrate your capability and fit for the role.
We think you need these skills to ace Regulatory Associate
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the key responsibilities and requirements for the Regulatory Associate position. Tailor your application to highlight how your skills and experiences align with these.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous experience in regulatory affairs or related fields. Mention specific tasks you've handled that relate to license maintenance, new marketing authorisations, or regulatory procedures.
Showcase Communication Skills: Since good communication skills are essential for this role, provide examples in your application of how you've effectively communicated with teams or external personnel in past roles.
Proofread Your Application: Before submitting, thoroughly proofread your application for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial in regulatory affairs.
How to prepare for a job interview at CK Group- Science, Clinical and Technical
✨Understand Regulatory Affairs
Make sure you have a solid grasp of the regulatory environment, especially in the pharmaceutical industry. Brush up on key concepts like license maintenance, marketing authorisations, and compliance with local regulations.
✨Showcase Your Communication Skills
Since good communication is crucial for this role, prepare to discuss how you've effectively communicated with external regulatory personnel in the past. Be ready to provide examples that highlight your ability to convey complex information clearly.
✨Demonstrate Teamwork and Results Focus
Prepare to talk about your experiences working in teams, particularly how you contributed to achieving results. Highlight any specific projects where your teamwork made a significant impact on regulatory objectives.
✨Be Ready for Technical Questions
Expect questions that assess your foundational knowledge of regulatory processes and IT skills. Review common regulatory procedures and be prepared to discuss how you would handle various scenarios related to license maintenance and filing.
