• Job Description

  Req#: R1430987

  Site Investigational Product Specialist/Research Nurse

  IQVIA cFSP

  Join us on our exciting journey!

  Remote/Hybrid/Office based working options.

  Our Sponsor Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward! The Site Investigational Product Specialist (SIPS) will serve as a subject matter expert for nursing administration as it relates to the process and procedure to develop Investigational Product Preparation and Administration Instructions IPPI, specific to drug administration in clinical research. The SIPS will play a lead role in the development of safe, efficient, and effective IP administration in clinical trials. The SIPS will be the key internal and external interface to ensure overall IPPI administration adherence.

  Job Overview:

  Co-author of the IPPI and review/provide input on all specific forms related to IP administration and dosing for all types of trials with an IPPI such as:

  • Administration routes (IV/SC/IM/intravesical/intraperitoneal/blood- and cell products, etc.)

  • IV access devices (central vs peripheral, Hickman, PICC, Port, PIV, midline, etc.)
  • Priming and flushing procedures
  • Filters
  • Hygienic standards
  • Medical devices (IV pumps, syringe pumps, plasma therm, etc.)

  Provide input in ancillary supply selection, Ancillary Supply Questionnaire and coordinate ancillary supply related questions in close collaboration with the Ancillary Support Associate (ASA)/ Site Manager (SM).

  Develop IP administration training materials.

  Support SM/IDM with resolving site IPPI related issues and site training (if applicable) according to local guidelines and blinding requirements.
  

  Responsible for internal team training of administration process for all versions of the IPPI according to internal Standard Operating Procedures (SOPs)/Work Instructions (WIs)/Instructions for Use (IFUs) and policies for internal staff.

  Support IPPI related initiatives and working groups. Actively participate in IPPI and all other nursing practice and scientific discussions. Track and integrate evolving trends in nursing practice into current and future IPPIs.

  
  

  Assist in site assessments/pre-trial assessment activities and study feasibility, providing recommendation from local area about site/investigator selection in collaboration with the trial team and develop IP related questions for site feasibility questionnaire
  

  Requirements:

  • A degree in general nursing is required.
  • 3- 4 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.
  • Experience in antibody treatment, (Oncology (hematology and solid tumor) and / or Immunology Therapeutic Area)
  • Experience with various IP administration routes (IV, SC, IM)
  • Clinical trial research experience.

  What is in it for you?

  • The chance to work on cutting edge medicines at the forefront of new medicines development.
  • We offer genuine career development opportunities for those who want to grow as part of the organisation.
  • We invest in keeping our teams stable, so workload is consistent.

  #LI-Remote

  IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com

• About the company

  IMS Health and Quintiles are now IQVIA. We are committed to providing solutions that enable healthcare companies to innovate with confidence, maximize opportunities and, ultimately, drive healthcare forward. We do this via breakthroughs in insights, t...

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