Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Pharmiweb.com RSS Feed PharmiWeb Candidate Blog

Pharmiweb.com RSS Feed PharmiWeb Client Blog

Job Details

Regulatory Officer / Scientific Writer

Company: Key People Limited
Location: Paris
Reference: 1506-9
Closing Date: 08 Dec 16
Type: Permanent
Salary (£): 20,000 - 30,000
Benefits: bonus and benefits

Job Summary:

An excellent opportunity has arisen for an experienced Regulatory Affairs professional / Regulatory Writer to join a leading Pharmaceutical company based in Paris.

Requirements:

An excellent opportunity has arisen for an experienced Regulatory Affairs professional / Regulatory Writer to join a leading Pharmaceutical company based in Paris.

Responsibilities:
• Plan the clinical development program
• Allocate appropriate resources for clinical studies
• Oversee the smooth conduct of clinical trials and publications
• Assist in the preparation and validation of clinical trial protocols
• Manage, train and supervise the team of Clinical Research Attaché based in France and the US
• Monitor the quality system (SOP) (write, update, validate) and train relevant staff
• Check the SOP in accordance with the requirements of society and the applicable regulatory requirements (ICH-GCP, the European Union directives, CFR)
• Follow the specifications in clinical monitoring provider companies

Experience Required:
• PharmD graduate with ideally MD or PhD
• Significant experience minimum 7 years in clinical research in a similar position
• Thorough knowledge of clinical development of regulations (EMA, FDA)
• CTA Experience for submissions with the EMA, FDA and national competent authorities
• Excellent verbal and written communication
• Excellent organizational and managerial skills
• Excellent computer skills and electronic applications
• essential fluent English

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

Key People is a recruitment consultancy with a reputation for providing good value that's been built up over 20 years. Clients come to us for three main reasons:

> We achieve results faster
> Our candidates really are a cut above
> We add greater value

We think it's because we're a private company driven by clients, not by shareholders.

For our candidates, we have developed relationships with thousands of clients nationwide, throughout Europe and also many around the globe, who choose to recruit through Key People, so you'll have a wide choice of opportunities to further your career. And, as we work for 75% of FTSE 100 companies, you'll get the chance to work for some prestigious, blue-chip organisations.

Apply for this job: Regulatory Officer / Scientific Writer

Contact Information:

Address:  Head Office
Catherine House
Adelaide Street
St Albans
Hertfordshire
AL3 5BA
England
Tel:  Tel: 44 (0) 1727 811634
Fax:  Fax: 44 (0) 1727 844838
Website:  Visit Our Web Site

Advertising
Share | | |
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.