Clinical Research Coordinator / Research Assistant / Research Nurse - Lyon

IQVIA; Paris; Sur place; EUR 30 000 - 40 000; Temps partiel

Résumé du poste

A leading global clinical research services provider in Paris is seeking a part-time Clinical Research Coordinator. This role involves supporting a medical device trial by monitoring device usage at patients' homes. Candidates should have a BS/BA in life sciences and relevant clinical experience. Strong IT and interpersonal skills are essential. Training will be provided.

Qualifications

• Relevant work experience in a clinical environment or medical setting.
• Basic knowledge of clinical trials and medical terminology.
• Strong IT competence with MS Windows and Office applications.
• Excellent interpersonal and organizational skills.

Responsabilités

• Support a clinical trial in monitoring a medical device.
• Visit patients in their homes for device monitoring.

Connaissances

Clinical Research

FDA Regulations

Data Collection

GCP

Infusion Experience

Phlebotomy

Clinical Trials

Pediatrics Experience

Qualitative Research Interviewing

Research Experience

Nursing

Epic

Formation

BS/BA in life sciences or educational equivalent

Outils

MS Windows

MS Office applications (Access, Outlook, Excel, Word)

Description du poste

Are you looking for an opportunity in Clinical Research Do you want to work for an industry leading company. If so come and join us - IQVIA are looking for a Clinical Research Coordinator.

This part-time role is to support a clinical trial in Lyon for a medical device trial where you will need to visit patients in their homes to monitor a medical device. Full training will be given.

We are looking for candidates with the following skills and experience :

• BS / BA in life sciences or educational equivalent and / or relevant work experience in a clinical environment or medical setting e.g. clinical research coordinator nurse medical assistant other medical profession
• Basic knowledge of clinical trials combined with in-depth knowledge of departmental protocol and study-specific operating procedures consent forms and study schedules
• Basic knowledge of medical terminology
• Strong IT competence skilled in using MS Windows and Office applications such as Access Outlook Excel and Word
• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers managers and client
• Good organizational skills with the ability to pay close attention to detail.

LI-DNP

LI-HCPN

LI-CES

LI-CT1

IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at

Required Experience :

Key Skills

Clinical Research,FDA Regulations,Data Collection,GCP,Infusion Experience,Phlebotomy,Clinical Trials,Pediatrics Experience,Qualitative Research Interviewing,Research Experience,Nursing,Epic

Employment Type : Part-Time

Experience : years

Vacancy : 1