Regulatory Submissions Manager

Key People

Sorry, This job post has expired.

Job ID :

3173


Company Type :

Staffing Firms


Industry :

Pharmaceuticals


Education Level :

Bsc


Address 1 :

United Kingdom,West London,West London,


Key Skills :

regulatory affairs, clinical, CRO, CTA, development, London, manager, SRO


Salary :

£50000 per annum


Date Posted :

26 Jul, 2016



Company Name :

Key People


Location1 :

West London




Job Category :

Regulatory Affairs Jobs


Experience :

Fresher


Job Type:

Permanent


Travel Amount:

negotiable





Description

My client, a leading Pharmaceutical company based in West London, is currently searching for a Regulatory Affairs Manager to join their team on a permanent basis. Within this role you will be responsible for ensuring the submissions of appropriate documentation to Regulatory Authorities globally prior to the performance of clinical trials and again prior to marketing of a new pharmaceutical product as well as any associated maintenance tasks.

Responsibilities:
- Responsible for the management of a team of regulatory professionals and/or responsible for timely preparation/coordination of regulatory submissions for a particular project
- Ensure that documents are prepared to the required standards by maintaining awareness of current regulatory standards related to drug submissions and clinical research
- Responsible for providing regulatory consultancy advice to client companies and/or the project team.
- Act as liaison between the client and Regulatory Authorities.
- Provide proactive interactions with all levels within the company and clients and will also be responsible for assisting other staff in business development activities related to regulatory submissions.

Experience required:
- Educated to BSc level or equivalent in pharmacy or a life sciences subject.
- Understanding of, and ability to determine relevance of, governmental regulatory processes and regulations as pertains to investigational drug regulation
- Excellent communication skills, organization and planning skills and attention to detail.
- Direct supervisory and project management skills and ability to work independently
- Significant experience in the pharmaceutical industry in Regulatory Affairs or possibly in Drug Development.

For further details about this role or other vacancies within Regulatory Affairs please contact Tim Barratt on +44(0)1727 817 626 or send a copy of your CV to tbarratt@keypeople.co.uk


Company Name:

Key People


Headquarters:

Catherine House,Adelaide Street


Sector:

Staffing Firms


Country:

United Kingdom


Zipcode:

AL3 5BA


Website:

www.keypeople.co.uk


Employees:

less than 100


Industry:

Pharmaceutical


City:

St Albans


Phone No. :

01727 817 626


Key People is a recognised leading supplier of staffing and recruitment services to the Pharmaceutical, Scientific & Biotech industry. The company has been operating for over 20 years and has an integrated team of qualified recruitment consultants averaging more than 7 years of recruitment experience. Each consultant is a specialist recruiter for their market area, so they can provide full market advice to candidates and clients alike.

For more information,visit www.keypeople.co.uk.

View all Key People Jobs



© 2019 Jobsinpharma - 4ward Technologies Ltd All rights reserved.