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Job Details

Regulatory Submissions Coordinator

Company: Regulatory Professionals
Location: Middlesex
Reference: J31215
Closing Date: 20 Dec 17
Type: Contract
Salary (£): Negotiable
Benefits: Attractive Daily rate

Job Summary:

A top 10 global CRO that work worldwide to provide full life cycle management in drug and biologic development are currently seeking an experienced Submissions Coordinator to join their established team.

Requirements:

Regulatory Submissions Coordinator

Middlesex

Attractive Daily Rate

A top 10 global CRO that work worldwide to provide full life cycle management in drug and biologic development are currently seeking an experienced Submissions Coordinator to join their established team. With the opportunity to work on a variety of therapeutic areas including cardiovascular and oncology products.

Responsibilities include:
* Prepare and review CTAs to UK and Ireland Regulatory Agencies
* Track submissions and ensure compliance to applicable regulations
* Provide advice on regulation and compliance changes

Application Requirements:
* Bachelor's Degree in life sciences
* A minimum of 3 years Regulatory Experience
* Hands on experience of preparing and reviewing CTAs
* UK & Ireland affiliate experience
* Experience of working with the MHRA
* Knowledge of Ethics Committee Submissions

Job Reference: J31215

Submissions, Regulator Affairs, Development, Clinical, Trial, Applications, CTA, Europe, EU, UK, Scotland, North, East, South, West, London, documentation, management, progression, career

Apply for this job: Regulatory Submissions Coordinator

Contact Information:

Address:  UK Office
3rd floor 33 Blagrave Street Reading
RG1 1LG
England
Tel:  +44 (0)118 9522 797
Website:  Visit Our Web Site

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