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Regulatory Medical Writer

Job Field:
Regulatory and Drug Safety Jobs
Discipline:
Regulatory Affairs Jobs
Country:
France
Region:
France All
Contract Type:
Permanent
Currency:
EUR
Salary:
45,000 to 65,000 per annum
Salary Description:
benefits
Posted:
12-Mar-19
Recruiter:
Key People
Job Ref:
1412-85

An excellent opportunity has arisen for a Medical Writer to join a pharmaceutical company based in Paris, specialising in the discovery, development, and commercialisation of novel targeted therapies, including cancer, chronic inflammatory diseases and neurological degenerative disorders.

You will work on a highly diverse range of projects including preparation of all types of regulatory and clinical study documentation.

Responsibilities include:
Medical writing of all types of regulatory and clinical study documentation including Investigators' Brochures, clinical study reports and protocols
Preparation of regulatory responses to health authorities
Preparation of marketing authorisation applications (eCTD module 2)
Simultaneously manage several projects and meet tight deadlines

Profile:
Previous medical or scientific writing experience is essential
Ability to analyse / summarise data from a diverse range of indications
Advanced scientific writing skills
Post-graduate science degree in a biomedical field
Experience in the preparation of marketing authorisation applications and regulatory responses would be advantageous
Fluency in written and spoken English

For further details, please contact Tim Barratt on +44(0)1727 817 626 or email tbarratt@keypeole.co.uk

Closing Date:
09/04/2019

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