At a Glance
- Tasks: Design and manage clinical trial labels while ensuring compliance with regulations.
- Company: Join ICON, a global leader in healthcare intelligence and clinical research.
- Benefits: Enjoy competitive salary, health coverage, and career development opportunities.
- Other info: Work remotely in a dynamic, inclusive environment with growth potential.
- Why this job: Make a real impact in healthcare by supporting innovative clinical trials.
- Qualifications: Bachelor's degree in relevant field and experience in clinical supply management.
The predicted salary is between 40000 - 50000 £ per year.
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients, and suppliers.
As a Senior Clinical Supply Specialist at ICON, you will oversee the management and distribution of clinical trial supplies, ensuring that all materials are delivered efficiently and in compliance with regulatory requirements.
What You Will Do:
- You will take ownership of clinical supplies and logistics deliverables, applying your expertise to complex challenges.
- Work within a global team.
- Create master label content according to existing processes and procedures, designing Clinical Trial labels.
- Perform quality critical checks of label content produced in various languages to required timelines.
- Perform quality critical checks of externally produced vendor label proofs prior to receipt by GSK.
- Creation of label documentation, required for in-country regulatory submissions, in a timely manner.
- Highlight label quality issues.
- Work with external vendors (translation service provider, component suppliers etc).
- Participate in GPM team meetings.
- Liaise with other groups within Clinical Manufacturing & Supply Chain.
Your Profile:
You will have a strong foundation in clinical supplies and logistics, with the experience to work independently and guide others.
Required qualifications and experience:
- Bachelor's degree in supply chain management, logistics, life sciences, or a related discipline.
- Significant experience in managing clinical supply, with a strong understanding of clinical trial requirements and regulatory standards.
- Experience within cGMP environment.
- Proficiency in supply chain management tools and data analysis, with experience in using software for tracking and reporting.
- Strong communication, interpersonal, and stakeholder management skills, with the ability to build effective partnerships and drive successful outcomes in a fast-paced environment.
Rewards & Benefits:
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include:
- Competitive base salary and performance related incentives.
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance programmes and wellbeing resources.
- Learning and development opportunities through structured training and career pathways.
Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility:
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Clinical Trial Pack Design Specialist – Label Creator employer: IRE
ICON is an exceptional employer that prioritises integrity, collaboration, and inclusion, creating a supportive work environment for its employees. As a Clinical Trial Pack Design Specialist, you will benefit from a competitive salary, comprehensive health and wellbeing programmes, and ample opportunities for professional growth through structured training. With a commitment to diversity and accessibility, ICON fosters a culture where every team member can thrive and contribute to the mission of delivering new medicines to patients faster.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Pack Design Specialist – Label Creator
✨Unlock Networking Opportunities
Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like IRE. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.
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✨Leverage Internships for Full-time Roles
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✨Tailor Your Approach
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We think you need these skills to ace Clinical Trial Pack Design Specialist – Label Creator
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at IRE!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show IRE that you're not just a fit for the job but also a safety-conscious candidate!
Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at IRE!
Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At IRE, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.
How to prepare for a job interview at IRE
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at IRE that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
✨Showcase Relevant Experience
If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
✨Know Their Products
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✨Be Ready for Regulatory Scenarios
In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
