At a Glance
- Tasks: Manage clinical biospecimens and ensure smooth execution of clinical study strategies.
- Company: Join ICON plc, a leading healthcare intelligence and clinical research organisation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
- Other info: Diverse culture focused on high performance and talent nurturing.
- Why this job: Make a real impact in clinical development while working in an inclusive environment.
- Qualifications: Science degree with experience in human sample management and lab design.
The predicted salary is between 40000 - 50000 £ per year.
ICON plc is a world‑leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
Fully embedded within a growing, global healthcare company, you will be responsible, with appropriate oversight from the Lead CBS, for the implementation and end‑to‑end operational execution of each GCO clinical study strategy as it relates to selected biospecimens samples.
Accountabilities:
- Contribute to providing input on clinical sample assessment sections in clinical trial‑related documents (such as protocols and consents).
- Create study‑specific sample collection tables and ensure alignment with blood volumes needed versus allowed.
- Liaise with internal stakeholders to provide input into the SSWs for safety and PK sample collection and testing needs.
- Responsible to set up and oversee the technical aspects of all laboratories involved in kit building, sample management and testing, including all related documentation such as lab manuals.
- Contribute to providing input and solutions on the ethical considerations for biospecimen collections and analyses for protocols and consents.
- Responsible for sample management and logistics with appropriate oversight from the Lead CBS.
Risk Management:
- In collaboration with the Lead CBS, ensure proper escalation of any identified trial specific risks and issues related to biospecimen collection and analysis in conjunction with relevant line functions.
Job requirements:
- Previous CRO or vendor experience.
- Must have human sample management, not just in‑vitro sample management or animal testing management.
- Must have an understanding of providing input on clinical sample assessments and requirements.
- Must have a background in understanding the design of a lab from the trial protocol perspective and would need to have systems experiences with the central labs to understand the build as well as Data transfer specification.
- Science degree.
- Lab background in terms of sample management, sample processing, understanding the assay requirements for the samples required for the assigned study.
- Kit design and protocol contribution.
- Must be open and able to communicate across multiple departments and line functions.
- Biospecimen management: Understand the requirement of collection of samples and which timepoints they are collected/ analyzed and data is analyzed.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well‑being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements.
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24‑hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.
- Life assurance.
- Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Clinical Biospecimen Scientist in Reading employer: ICON
ICON plc is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration within the healthcare intelligence and clinical research sector. With a strong commitment to employee growth, you will have access to mentorship opportunities and the chance to lead diverse teams, all while enjoying the flexibility of travel and a supportive environment that values your contributions.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Biospecimen Scientist in Reading
✨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 Clinical Biospecimen Scientist role.
✨Tip Number 2
Prepare for those interviews by brushing up on your knowledge of biospecimen management and lab protocols. We recommend practising common interview questions and even doing mock interviews with friends or mentors to boost your confidence.
✨Tip Number 3
Showcase your passion for the role! When you get the chance to speak with recruiters or during interviews, let them know why you’re excited about contributing to clinical studies and how your background aligns with their mission at ICON.
✨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 love seeing candidates who take the initiative to engage directly with us.
We think you need these skills to ace Clinical Biospecimen Scientist in Reading
Some tips for your application 🫡
Tailor Your Application:Make sure to customise your CV and cover letter for the Clinical Biospecimen Scientist role. Highlight your relevant experience in human sample management and any specific projects that align with the job description.
Showcase Your Skills:Don’t forget to emphasise your technical skills and lab background. Mention any experience you have with sample management, kit design, and your understanding of clinical trial protocols to really stand out.
Be Clear and Concise:Keep your application clear and to the point. Use bullet points where possible to make it easy for us to see your qualifications and experiences at a glance. We love a well-organised application!
Apply Through Our Website:We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets into the right hands and helps us get to know you better!
How to prepare for a job interview at ICON
✨Know Your Biospecimens
Make sure you brush up on your knowledge of biospecimen management and the specific requirements for clinical trials. Be ready to discuss how you've handled sample collection, processing, and logistics in previous roles, as this will show your understanding of the job's core responsibilities.
✨Understand the Protocols
Familiarise yourself with the typical protocols and consents related to clinical studies. Being able to articulate how you would contribute to these documents will demonstrate your proactive approach and readiness to engage with the team.
✨Showcase Your Collaboration Skills
Since the role involves liaising with multiple departments, prepare examples of how you've successfully collaborated in the past. Highlight any experience you have in cross-functional teams, especially in a CRO or similar environment, to illustrate your ability to communicate effectively.
✨Prepare for Ethical Discussions
Be prepared to discuss ethical considerations surrounding biospecimen collection and analysis. Think about scenarios where you had to navigate ethical dilemmas and how you approached them, as this will reflect your critical thinking and integrity in the field.
