Research Nurse – Local Contractor

This is a fully remote position, open to applicants in France.

📋 Description

• Be thoroughly familiar with the trial protocol, Case Report Forms (CRFs/eCRF), off-site manual (if applicable), supporting documents, procedures, and timelines to facilitate the daily operations of the trial, including all pertinent SOPs.

• Effectively communicate with the Illingworth Research Nurse Project Manager (RNPM), Research Nurse Manager, site personnel, and the Principal Investigator to ensure a seamless and efficient flow of information.

• Maintain precise documentation, including electronic data transfers in accordance with Illingworth SOPs throughout the trial, ensuring participant confidentiality and adherence to GCP and data protection regulations.

• Attend Site Initiation Visits (SIVs) as necessary and participate in additional meetings, including multidisciplinary, project management, and client-facing discussions.

• Coordinate (in collaboration with the RN team) and complete subject trial visits both on-site and off-site.

• Ensure that all trial-related procedures and assessments are conducted in line with the protocol and relevant SOPs, and that data is collected accurately.

• Administer trial medication in accordance with the protocol and ensure the safe storage, transfer, and accountability of trial medication as per Illingworth SOPs.

• Process, securely package, and dispatch samples, coordinating with courier services and partner organizations in line with project requirements and supporting documentation.

• Assist in identifying potentially eligible patients for research projects and support patient recruitment into clinical trials, providing information and assistance for care both on-site and off-site.

• Ensure accurate reporting of adverse events (AEs) and serious adverse events (SAEs)/suspected unexpected serious adverse reactions (SUSARs) to the site team and relevant RNPM, and offer support for any necessary follow-up.

• Report any suspected misconduct or fraud to Illingworth and affiliated companies.

⛳️ Requirements

• Registered nurse with at least 2 years of post-qualification experience.

• Experience in research and clinical trials with GCP certification.

• Familiarity with research design and methodology is advantageous.

• Preferred experience and proficiency in clinical nursing procedures such as venepuncture and ECG.

• Ability to work independently and take initiative while effectively collaborating within a multidisciplinary team.

• Exceptional verbal and written communication skills.

• Capacity to prioritize and manage multiple tasks efficiently.

• Proficient working knowledge of computer software, including Outlook, Word, Excel, and PowerPoint at a minimum.

🏝️ Benefits

• Health insurance

• 401(k) matching

• Flexible working hours

• Paid time off

• Remote work options