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- Tasks: Join us in preparing and administering investigational products for clinical trials.
- Company: ICON plc, a leading healthcare intelligence and clinical research organisation.
- Benefits: Competitive salary, health insurance, flexible benefits, and global support programmes.
- Why this job: Make a real impact in oncology while working with innovative teams.
- Qualifications: Degree in nursing and experience in clinical trials and IP administration required.
- Other info: Inclusive culture that values diversity and offers excellent career growth opportunities.
The predicted salary is between 36000 - 60000 £ 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.
As a Site Investigational Product Specialist, you will be dedicated to one of our global pharmaceutical clients, a company that values performance, recognises merit and has a high focus on quality. This environment encourages innovation, individuality and embraces people that want to be a part of it.
The Site Investigational Product Specialist will serve as a key contact point between the sponsor and the investigational site for Investigational Product Preparation Instructions (IPPI) training of studies with a complex IP preparation process. This role will focus on IPPI review and training/implementation of IP preparation steps for all compounds deemed requiring training plans. The Site Investigational Product Specialist will be the key internal and external interface to ensure overall IPPI adherence. He/she will contribute to continuous process improvement, training and mentoring for IPPI.
The tasks undertaken are varied and can include:
- Play a key role in the safe, efficient and effective Investigational Product preparation and administration in clinical trials.
- Review and provide input on Investigational Product Preparation Instructions, Site Investigational Product Procedures Manual, monitoring guidelines and all specific forms related to Investigational Product preparation and dosing before finalization as applicable.
- Process risk assessment review where applicable.
- Close collaboration with the Drug Product Development team and the Drug Preparation Administration Team.
- Early connection with investigational site pharmacy and nursing staff to review site IP process and equipment.
- Close collaboration with (Global Trial Lead) GTL, (Study Manager) SM, (Trial Manager) TM, Independent Drug Monitor (IDM) and Pharmacy Investigational Product Specialist (PIPS) for all IPPI related topics.
- Evaluate and support process for IP ancillary supplies/administration kits are compatible with the site equipment/practice in the country/investigational site.
- Review of site's dispensing and accountability records to ensure key information is captured to confirm dose delivery and administration is documented e.g. infusion rates/volumes.
- Collaboration on Investigational Product training material development with key stakeholders.
- Observe first dosing on site and/or support SM/IDM/PIPS if allowed according to local guidelines and blinding requirements.
- Point of contact for the internal study team in the country for questions related to the IP administration.
- Review any modification of IPPI, SIPPM manual, specific forms related to IP administration and dosing during the applicable phases of the trial.
- Establish and maintain good and productive working relationships with internal and external stakeholders (e.g. nurses, investigators,…).
You are:
- A degree in general nursing is required.
- 3-4 years of recent clinical/hospital experience is required.
- Experience in antibody treatment, (Oncology (hematology and solid tumor) and/or Immunology Therapeutic Area).
- Minimum of 5+ years of recent clinical/hospital experience is required; however, other relevant experience may be considered by the hiring manager when considering the candidate’s eligibility.
- Minimum of 5+ years’ experience with various IP administration routes (IV, SC, IM, intravesical, intraperitoneal, blood- and cell products) and priming and flushing procedures required.
- Extensive knowledge on Administration related requirements (background of anatomy and physiology, metabolism of drugs and IP, hygienic requirements, how to handle hazardous drugs).
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 here.
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.
IP Administration - Oncology Nurse in Reading employer: ICON
Contact Detail:
ICON Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land IP Administration - Oncology Nurse in Reading
✨Tip Number 1
Network like a pro! Reach out to your connections in the healthcare and clinical research fields. Attend industry events or webinars, and don’t be shy about introducing yourself. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their mission and values, especially around innovation and quality. Tailor your responses to show how your experience aligns with their goals – it’ll make you stand out!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors. Focus on articulating your clinical experience and how it relates to the role of an IP Administrator. The more comfortable you are, the better you’ll perform when it counts.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage directly with us. So, go ahead and submit that application!
We think you need these skills to ace IP Administration - Oncology Nurse in Reading
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the IP Administration role. Highlight your nursing experience, especially in oncology and clinical trials, and showcase any relevant skills that match the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about this role and how your background makes you a perfect fit. Don’t forget to mention your experience with investigational products!
Showcase Your Teamwork Skills: Collaboration is key in this role, so be sure to include examples of how you've worked effectively with other healthcare professionals. Mention any specific projects or experiences where teamwork led to successful outcomes.
Apply Through Our Website: We encourage you to apply directly 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 to do!
How to prepare for a job interview at ICON
✨Know Your IP Inside Out
Make sure you have a solid understanding of Investigational Product Preparation Instructions (IPPI) and the specific processes involved in IP administration. Brush up on your knowledge of various administration routes like IV, SC, and IM, as well as any relevant guidelines or protocols that may come up during the interview.
✨Showcase Your Clinical Experience
Highlight your clinical experience, especially in oncology or immunology. Be prepared to discuss specific cases where you've successfully managed IP administration or collaborated with nursing staff and pharmacy teams. This will demonstrate your hands-on expertise and ability to work in a clinical trial environment.
✨Prepare for Scenario-Based Questions
Expect scenario-based questions that assess your problem-solving skills and ability to handle complex situations. Think about past experiences where you had to adapt quickly or implement training plans, and be ready to share those stories to illustrate your critical thinking and adaptability.
✨Emphasise Team Collaboration
Since this role involves close collaboration with various stakeholders, be sure to express your teamwork skills. Share examples of how you've built productive relationships with colleagues, investigators, and external partners, and how you’ve contributed to a positive team dynamic in previous roles.
