Site Investigational Product Specialist

ICON Strategic Solutions; United Kingdom; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading clinical research organization in the UK is seeking a Site Investigational Product Specialist to serve as the key contact between sponsors and investigational sites. The role requires a degree in general nursing and 3-4 years of recent clinical experience, focusing on the preparation and administration of investigational products in clinical trials. This position offers competitive compensation and various benefits aimed at fostering a diverse and inclusive work environment.

Benefits

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme

Life assurance

Childcare vouchers

Qualifications

• Minimum 3-4 years of recent clinical/hospital experience.
• 5+ years of experience in clinical/hospital settings is preferred.
• Extensive knowledge of anatomy, physiology, and drug handling procedures.

Responsibilities

• Act as a key contact between sponsor and investigational site for IP training.
• Review IP preparation instructions and collaborate with development teams.
• Conduct risk assessments and trainings related to investigational product administration.

Skills

Clinical trial research experience

Experience in antibody treatment

Oncology (hematology and solid tumour) knowledge

Immunology Therapeutic Area knowledge

Administration of IP routes (IV, SC, IM)

Education

Degree in general nursing

Job description

Site Investigational Product Specialist

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 joining the world’s largest and most comprehensive clinical research organisation, powered by healthcare intelligence.

What you will be doing

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 finalisation 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 tumour) and/or Immunology Therapeutic Area.
• Minimum 3 years’ experience with various IP administration routes (IV, SC, IM).
• Clinical trial research experience.
• 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 prime 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 maximise 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 specialised 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, subsidised travel passes, health assessments, among others.

Visit our careers site to read more about the benefits ICON offers.

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, colour, 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.

Are you a current ICON Employee? Please click here to apply.