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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 competitive pay, potential for remote work, and valuable industry experience.
- Why this job: Be part of a mission-driven team making a real impact in healthcare.
- Qualifications: A relevant scientific degree and basic knowledge of the regulatory environment are required.
- Other info: This is a 12-month contract role based in Basingstoke; DBS check may apply.
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 136 593 in all correspondence.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Regulatory Associate employer: CK Group
Contact Detail:
CK Group 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 the nuances of license maintenance activities and marketing authorisations will give you an edge during discussions.
✨Tip Number 2
Network with professionals already working in regulatory affairs. Attend industry events or join relevant online forums to build connections that could provide insights or even referrals for the role.
✨Tip Number 3
Brush up on your communication skills, as this role requires effective interaction with external regulatory personnel. Practising clear and concise communication can help you stand out during interviews.
✨Tip Number 4
Demonstrate your team working abilities by sharing examples of past collaborative projects. Highlighting your focus on results will resonate well with the hiring team looking for operational excellence.
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 aspects.
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 stakeholders in past positions.
Proofread Your Application: Before submitting, thoroughly proofread your application materials. Ensure there are no spelling or grammatical errors, as attention to detail is crucial in regulatory affairs.
How to prepare for a job interview at CK Group
✨Understand Regulatory Affairs Basics
Make sure you have a solid grasp of the regulatory environment in the pharmaceutical industry. Brush up on key concepts like license maintenance, marketing authorisations, and compliance with local regulations, as these will likely come up during your interview.
✨Showcase Your Communication Skills
Since good communication is essential for this role, prepare to discuss examples where you've effectively communicated complex information. Think about times when you’ve facilitated relationships with external personnel or worked within a team to achieve results.
✨Demonstrate IT Proficiency
Be ready to talk about your computer and IT skills, especially any experience with regulatory tracking systems or document management. Highlight any specific software you’ve used that relates to regulatory affairs, as this could set you apart from other candidates.
✨Prepare for Scenario-Based Questions
Expect questions that assess how you would handle specific regulatory challenges. Prepare by thinking through potential scenarios related to labelling changes or CMC changes, and how you would approach them to ensure compliance and operational excellence.
