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- Tasks: Lead and manage clinical studies for animal health products in a quality-focused environment.
- Company: Join a leading research and development team in Newry.
- Benefits: Enjoy 32 days annual leave, healthcare cash plan, and career development opportunities.
- Other info: Permanent position with excellent perks and a supportive work culture.
- Why this job: Make a real impact in animal health while working with a dynamic team.
- Qualifications: Degree in life sciences and strong communication skills required.
The predicted salary is between 46000 - 52000 £ per year.
An opportunity has arisen for the position of Study Director, working in the Clinical Section of the Research & Development Department.
Main Activities/Tasks:
- The Study Director will work in a quality focus environment regulated to GLP standards.
- The successful candidate will lead, manage data and report non-clinical and clinical studies for safety and efficacy trials for animal health products.
- The successful candidate will be responsible for the planning, conduct and reporting of studies in an organised and timely manner, and in a Quality focus environment in accordance with Regulatory requirements (e.g. FDA/EMA), the principles of GLP, GCP, and SOPs in operation within the Research & Development Department.
- You will be responsible for a wide range of study designs, including:
- Pharmacokinetic/Bioequivalence studies.
- Residue depletion studies.
- Target Animal Safety.
- Laboratory Studies (dissolution and characterisation).
- Clinical studies (artificial and natural infections).
Essential Criteria:
- Educated to a minimum of degree level in a relevant life science discipline.
- Flexible and able to prioritise and time manage efficiently.
- Proven commitment to work to defined deadlines.
- Excellent written and verbal communication.
- Good interpersonal skills.
- Assertive yet tactful.
- Possess a strong team spirit with the ability to work as part of a multi-disciplined team.
- Have a full UK driving licence.
Desirable Criteria:
- Have previous experience in the role.
- Have previously worked in a GLP/GMP environment.
- Have previous experience in in vitro experiments/models.
- Previous experience in a laboratory with knowledge of bioanalytical method testing.
- Have understanding of relevant regulatory guidelines.
Benefits:
- Free life assurance
- Pension salary sacrifice scheme with 5% employer contribution
- Healthcare cash plan
- 32 days annual leave (increasing with length of service)
- Wedding leave
- Enhanced Maternity / Paternity Pay
- Company Sick Pay
- Subsidised Canteen Facilities
- FREE On-site parking
- Cycle to Work Scheme
- Tech Purchase Scheme
- Free Will-Writing Service
- Employee perks/discounts scheme
- Employee Assistance Programme (EAP)
- Employee well-being initiatives
- Employee recognition scheme
- Career development opportunities
Contact: To Apply Please forward your CV via the APPLY Now button below.
Clinical Study Director TLNT1_NI employer: Norbrook
Contact Detail:
Norbrook Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Study Director TLNT1_NI
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and understanding their values. We recommend practising common interview questions and even role-playing with a friend. The more prepared you are, the more confident you'll feel when it’s time to shine!
✨Tip Number 3
Follow up after interviews! A simple thank-you email can go a long way in showing your appreciation and keeping you top of mind. We suggest mentioning something specific from the interview to make it personal and memorable.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we often have exclusive opportunities listed there that you won’t find anywhere else.
We think you need these skills to ace Clinical Study Director TLNT1_NI
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Study Director role. Highlight your relevant experience in GLP environments and any specific studies you've managed. We want to see how your background aligns with our needs!
Showcase Your Communication Skills: Since excellent written communication is key for this role, ensure your application is clear and concise. Use bullet points where necessary and avoid jargon unless it's relevant to the position. We appreciate straightforwardness!
Highlight Team Spirit: We’re looking for someone who can work well in a multi-disciplined team. Share examples of how you’ve collaborated with others in past roles. This will show us that you’re not just a lone wolf but a team player!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just hit that APPLY Now button!
How to prepare for a job interview at Norbrook
✨Know Your GLP and GCP Standards
Make sure you brush up on Good Laboratory Practice (GLP) and Good Clinical Practice (GCP) standards. Being able to discuss how these principles apply to your work will show that you’re not just familiar with the regulations, but that you can also implement them effectively in your role.
✨Demonstrate Your Team Spirit
Since this role requires working as part of a multi-disciplined team, be ready to share examples of how you've successfully collaborated with others in the past. Highlight your interpersonal skills and how you balance assertiveness with tact when working with colleagues.
✨Prepare for Technical Questions
Expect questions about specific study designs like pharmacokinetic studies or residue depletion studies. Brush up on your technical knowledge and be prepared to discuss any relevant experience you have in these areas, especially if you’ve worked in a GLP/GMP environment.
✨Showcase Your Time Management Skills
The ability to prioritise and manage time efficiently is crucial for this role. Be prepared to discuss how you handle tight deadlines and organise your workload. Sharing a specific example where you successfully managed multiple tasks can really make you stand out.