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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 regulatory environments 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 136 593 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
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 licensing, labelling changes, and CMC (Chemistry, Manufacturing, and Controls) will give you an edge during interviews.
✨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 insights into the role and may even lead to referrals.
✨Tip Number 3
Brush up on your communication skills, as they are crucial for this role. Practice articulating complex regulatory concepts clearly and concisely, as you may need to explain these to non-experts.
✨Tip Number 4
Demonstrate your ability to work in a team by sharing examples from your past experiences. Highlight how you’ve collaborated with others to achieve results, as teamwork is essential in regulatory affairs.
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, regulatory procedures, or communication with regulatory bodies.
Showcase Your Qualifications: Make sure to mention your Bachelor’s degree or equivalent in a relevant scientific subject. If you have any additional certifications or training related to regulatory affairs, include those as well.
Proofread Your Application: Before submitting, thoroughly proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail.
How to prepare for a job interview at CK Group
✨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 licensing, labelling changes, and marketing authorisations, as these will likely come up during your interview.
✨Showcase Your Communication Skills
Since good communication is crucial for this role, prepare to demonstrate your ability to convey complex information clearly. Think of examples where you've successfully communicated with team members or external stakeholders.
✨Highlight Teamwork Experience
This position requires strong teamwork skills, so be ready to discuss your experiences working in teams. Share specific instances where you contributed to achieving results as part of a group.
✨Prepare for Technical Questions
Expect technical questions related to regulatory procedures and compliance. Review common regulatory practices and be prepared to discuss how you would handle various scenarios that may arise in the role.
