Research Nurse – Per Diem

Role Overview

• Fully conversant with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to enable day to day running of the trial including all relevant SOPs
• Communicate effectively with the Illingworth research nurse project manager (RNPM), Research nurse manager, site staff and the Principal Investigator, to ensure a smooth and efficient flow of information
• Maintain accurate documentation including electronic transfer of data as per Illingworth SOPs throughout the trial, ensuring subject confidentiality, adhering to GCP and data protection requirements
• Attend Site Initiation Visits (SIV) as required and any other necessary meetings, including multi-disciplinary, project management and client-facing meetings
• Coordinate (working with the RN team) and complete subject trial visits on
• and off-site
• Ensure all trial related procedures and assessments are completed according to the protocol and relevant SOPs and that data is collected accurately
• Administer trial medication as per the protocol, and facilitate the safe storage, transfer, and accountability of trial medication in accordance with Illingworth SOPs
• Process and safely package and dispatch samples, liaising with courier companies and organizations in line with project requirements and supporting documents
• Assist in identifying potentially eligible patients for research projects and assist with patient recruitment into clinical trials providing information and support for those patients for on
• and off-site care
• Ensure the accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, providing support for any additional follow-up that may be required
• Report any suspected misconduct or fraud to Illingworth and associated companies

Requirements

• Registered nurse with a minimum of 2 years' post qualification experience
• Research and clinical trials experience with GCP certification
• Knowledge of research design and methodology desirable
• Experience and knowledge of clinical nursing skills such as Venepuncture and ECG preferable
• Ability to work autonomously with initiative in a team within a multidisciplinary environment
• Excellent verbal and written communication skills
• Ability to prioritize and manage multiple tasks
• Good working knowledge of computer software including Outlook, Word, Excel, and PowerPoint as a minimum

Tech Stack

• Google Cloud Platform

Benefits

• company car or car allowance
• Health benefits to include Medical, Dental and Vision
• Company match 401k
• eligibility to participate in Employee Stock Purchase Plan
• Eligibility to earn commissions/bonus based on company and individual performance
• flexible paid time off (PTO) and sick time