This site uses cookies. By continuing to browse the site you are agreeing to our use of cookies. Find out more here.

Close Message
NextPharmaJob.com for pharmaceutical industry jobs
NonStop Recruitment
NextPharmaJob.com is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Senior Labeling Engineer - fast paced role - FDA timelines
Switzerland
Contract Opportunity - Pharmacovigilance Medical Director
London
Pharmacovigilance- SDEA Specialist
United Kingdom
Pharmacovigilance PV Officer
North West
Pharmacovigilance Associate
South East
More...

To receive a FREE weekly email alert of all the latest pharmaceutical industry jobs added to our database enter your email address below.

Submit | Tell me more...

Sister sites:
Our sister site Our sister site
Partner sites:

At Burntsky Limited we work with a number of third parties in order to maximise the reach of the jobs posted with us including but not limited to:

JooblePartner Jooble
UK Jobs
Science Jobs

Job Details
Options
back Back    save job Save Job      apply for job Apply Online      contact recruiter Contact Recruiter            print Print

Contract Opportunity - Pharmacovigilance Medical Director



Business Type: Pharmaceutical Company
Job Type: Pharmacovigilance
Job Level: Management
Position: Full Time
Location: London
Reference: HM156430/4.
Closing Date: 16/07/17
Background:

New Contract - Pharmacovigilance Medical Director

Our client is one of the most well established pharmaceuticals in the world, that promote an exciting ever, developing, start up mentality. We are currently looking for an experience PV Physician to join on contract in post as a Pharmacovigilance Medical Director.

Your responsibility will include:

  • Membership of teams/committees for developmental and marketed compounds as necessary. Support and contribute to all facets of safety review/safety expertise departmentally, inter-departmentally and at corporate level
  • Contribute/review PSURs and other aggregate safety documents/RMPs
  • Contribute to the development of SDEAs as needed
  • Support all applicable PV regulations and, as appropriate, be cognizant of the requirements around the QPPV Case review, both for ''own'' compounds and more generally as needed.
  • Working knowledge and familiarity with clinical protocols, SAPs, study reports and aggregate safety reports.

GMC registration is essential, and previous experience in Pharmacovigilance development.

Call me Harriet Maidman at NonStop Recruitment now for a confidential conversation. Contact me on h.maidman@nonstop-pharma.com or 0207 940 2103. Please send your CV in word format OR if this does not sound like the opportunity for you, please do get in touch speculatively and we can discuss your next career move, and potential options



NonStop Recruitment Posted by:: NonStop Recruitment (View all our vacancies)
Unless otherwise stated, if applying for a job, you must ensure that you are already authorised to work in the country in which the job is based
Posted: 09/07/2017 | NPJ Ref: 189189
line graphic

Compatible with:

JobMate   Broadbean   Idibu

Site optimised for Internet Explorer 8+ / Firefox 3+
View a complete Jobs Listing




Credit cards image