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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.
Additional Information:
Applicants should be able to provide proof that they have a right to work in the UK at the time of their application. Applicants who are unable to provide this proof will not be considered. We regret that applications received after the closing date and time will not be accepted. We are unable to sponsor or take over sponsorship of a Visa at this time. This role is based on a site that produces penicillin and as such, would not be suitable for those with a penicillin allergy.
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 employer: Norbrook
Contact Detail:
Norbrook Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Study Director
✨Tip Number 1
Network like a pro! Reach out to professionals in the clinical research field on LinkedIn or at industry events. 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 practising common questions related to clinical studies and GLP standards. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Showcase your passion for animal health products and clinical research during interviews. We want to see your enthusiasm and commitment to the field, so don’t hold back on sharing your experiences and insights!
✨Tip Number 4
Apply through our website for a smoother process! We’ve made it easy for you to submit your application and get noticed. Plus, it shows you’re genuinely interested in joining our team.
We think you need these skills to ace Clinical Study Director
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/GMP 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 and verbal communication is key for this role, ensure your application reflects this. Use clear, concise language and structure your CV and cover letter well. We love a good, organised presentation!
Highlight Team Spirit: We’re all about teamwork here at StudySmarter! Make sure to mention any experiences where you’ve worked as part of a multi-disciplined team. Show us how you can contribute to our collaborative environment.
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 before your interview. Being able to discuss how these principles apply to the role of a Clinical Study Director will show that you’re not just familiar with the regulations, but that you can also implement them effectively.
✨Demonstrate Your Team Spirit
Since this role requires working as part of a multi-disciplined team, be prepared to share examples of how you've successfully collaborated in the past. Highlight your interpersonal skills and how you balance assertiveness with tact to foster a positive team environment.
✨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 ready to discuss any relevant experience you have in these areas. This will help you stand out as a candidate who is not only qualified but also passionate about the work.
✨Showcase Your Time Management Skills
The ability to prioritise and manage time efficiently is crucial for this role. Be ready to discuss how you’ve handled tight deadlines in previous positions. Use specific examples to illustrate your commitment to meeting deadlines while maintaining quality in your work.