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

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Regulatory Affairs Specialist- KIEV

Company: i-Pharm Consulting
Location: Kiev
Reference: BN12222
Closing Date: 26 Feb 18
Type: Permanent
Salary (£): Negotiable
Benefits:

Job Summary:

Regulatory Affairs Specialist needed in UkraineWell- settled and innovative CRO is looking for a Regulatory Affairs Specialist.If you have at least 3 years of experience within local submissions, new drugs registration, click here to apply and find out more.

Requirements:

Regulatory Affairs Specialist needed in Ukraine
Well- settled and innovative CRO is looking for a Regulatory Affairs Specialist.
If you have at least 3 years of experience within local submissions, new drugs registration, click here to apply and find out more.

JOB TITLE
Regulatory Affairs Consultant/ new drugs registration/ GMP / local authorities submissions

LOCATION
Kiev- Ukraine

BENEFITS
Competitive salary+ benefits
Great work-environment
Innovative CRO
Clear career path


ROLE/DESCRIPTION

You will perform as a Regulatory Affairs Associate for a CRO. If you have experience within drug registration, GMP and local submission, do not hesitate to let us know. While working with the world- leading sponsors, you will be able to influence the pharmaceutical market of women’s health within genecology, breast cancer and more.
Clear scope of duties and career path will enable you to organise your work in a preferable way and perform as an autonomous independent.



REQUIREMENTS
Location: Kiev
Medical/Scientific degree
3+ years of Regulatory Affairs experience within drug registration, GMP, women’s health
Ukrainian+ English fluent

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical around the globe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.

www.i-pharmconsulting.com


TO APPLY

If you would like to discuss this vacancy further, please call Consultant, Monika Naturalna on + 44 (0) 20 3873 7068, mnaturalna@i-pharmconsulting.com. If this role is not suitable, Monika is also available to discuss other possible positions or answer any general questions regarding your career and the current market.


KEY WORDS
Clinical Trials/ Regulatory Affairs/ Regulatory Lead/ Regulatory Affairs Associate/

Apply for this job: Regulatory Affairs Specialist- KIEV

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

Advertising
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.