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Job Details

Senior Medical Writer

Company: i-Pharm Consulting
Location: Spain
Reference: NIB0001
Closing Date: 01 Sep 17
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Senior Medical Writer – Home-basedAn exciting opportunity to join a fast paced and dynamic team in one of the leading CROs in the world. The Senior Medical Writer researches, creates and edits all documents relating to clinical trials. You will be the primary contact for medical writing projects, setting timelines, providing leadership and running training to support more junior writing staff. ...

Requirements:

Senior Medical Writer – Home-based

An exciting opportunity to join a fast paced and dynamic team in one of the leading CROs in the world. The Senior Medical Writer researches, creates and edits all documents relating to clinical trials. You will be the primary contact for medical writing projects, setting timelines, providing leadership and running training to support more junior writing staff.

Job Title: Senior Medical Writer
Location: UK/ England / Dublin / Home-based
Benefits: Above market rate salary + performance bonus + corporate benefits package

Job Responsibilities:
• Write clinical documents for submission to regulatory authorities
. Experience leading CSR's & Protocols
• Perform literature reviews and searches to obtain background information for document creation.

Ideal Candidate:
The ideal candidate will have at least 3 years of years experience as a medical writer. Writing multiple clinical study reports and either CTD documents or similar study protocols. Very good communication skills are essential and a client focused approach is to work is necessary.

TO APPLY
If you would like to discuss this vacancy further, please call Senior Regulatory Recruitment Consultant Niall Behan on +44 (0)20 3189 0463, or email nbehan@i-pharmconsulting.com. If this role is not suitable, Niall is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


KEY WORDS
Regulatory affairs, senior regulatory affairs executive, senior regulatory affairs, clinical regulatory affairs, reg affairs, regulatory affairs manager, regulatory affairs senior manager, regulatory affairs director, development, regulatory affairs manager, regulatory intelligence, Cambridgeshire, Cambridge, Hertford, Hertfordshire, London, East of England, London, West London, Uxbridge, Maidenhead, Slough, Reading


Apply for this job: Senior Medical Writer

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

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