Clinical Site Associate- Paris- France

CDI | Tremblay en France, LE DE FRANCE | 4 mois | Date limite: 18 mai 2018 00h 00min 00s
Cette position a expiré. Ne pas appliquer!

Résumé de l'emploi

CDI
; Negotiable

Description de poste


Job Details
New Search Return to Search Previous Job Next Job Send to a Friend
Job 179 of 1000
Clinical Site Associate- Paris- France

Company: i-Pharm Consulting
Location: France
Reference: 12200452018
Closing Date: 18 May 18
Type: Permanent
Salary (£): Negotiable
Benefits:


Job Summary:

Clinical Site AssociateOne of Pharma marker-leading CRO is looking for autonomous, independent and passionate Clinical Site Associate in Paris.This position is exceptional. Performing monitoring activities, you will quickly notice that your job is not just a routine that you already know, but the job organization is allowing you to truly develop your management skills and autonomous approach.


Requirements:

Clinical Site Associate
One of Pharma marker-leading CRO is looking for autonomous, independent and passionate Clinical Site Associate in Paris.
This position is exceptional. Performing monitoring activities, you will quickly notice that your job is not just a routine that you already know, but the job organization is allowing you to truly develop your management skills and autonomous approach.
LOCATION
France- Paris
ROLE/DESCRIPTION
Suitable candidate should have 1 to 2 years’ experience working as a clinical research associate in varying therapeutic area. The position is dedicated to one sponsor, market leader in various therapy areas studies. Thanks to that you can develop both with a specific sponsor and once of the best market CROs. As a part of international team, you’ll be involved in different activities including study start up, routine monitoring and close-out of clinical sites. You’ll be involved in project work, managing small projects and reviewing project progress. This position is unique regarding travel, the monitoring visits are within the comfortable average of 5-7 per month.
COMPANY
This CRO is one of the world’s most dynamic, with progression and career development high on their list of priorities. The company has 10,000+ employees and operations in more than 30 countries globally. Trials are ongoing in a broad range of therapeutic areas including: Oncology, Neurology, Respiratory, Cardiovascular, Respiratory and Infectious Disease.
The Role: Clinical Site Associate
REQUIREMENTS
* Bachelor of Science or Bachelor of Nursing Degree
* 1+ years independent monitoring experience
* Entitlement to work in the France
* Driving Licence
* Fluency in French and English
BENEFITS
* Excellent salary
* Healthcare
* Life Assurance
* Work-Life Balance
* Reduced number of protocols
* Reduced on-site monitoring
ABOUT i-PHARM CONSULTING
i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
www.i-pharmconsulting.com
TO APPLY
If you would like to discuss this vacancy further, please call Principal Consultant Monika Naturalna on (+44) 020 3873 7068, or email mnaturalna@i-pharmconsulting.com. If this role is not suitable, Monika is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
KEY WORDS
CRA / Clinical Monitor / France / Paris / Permanent / CRO / Monitoring / CRA I / CRA II / CRA1 / CRA2 / Clinical Site/ Management


Contact Information:
Address:  Head Office
212 New King’s Road London
SW6 4NZ
England
Reasons to work for i-Pharm Consulting
Tel:  +44 (0) 20 3189 2299
Website:  Visit Our Web Site

New Search Return to Search Previous Job Next Job Send to a Friend

Emplois Similaires