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

Close Message for pharmaceutical industry jobs
i-Pharm Consulting is dedicated to putting job seekers looking for pharmaceutical industry jobs in touch with recruiters and employers.

Similar jobs you may be interested in:

Chargé de Pharmacovigilance - CDD 10 Mois
Associate Safety Director- Pharmaceutical
Chargé de Pharmacovigilance - Nord - proche Belgique
Chargé de Pharmacovigilance - Nord - proche Belgique
pharmacien AQ, RA , PV- Gérez un projet de A à Z

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
This job has expired. Click here to view similar jobs.

Principal Pharmacovigilance Scientist

Business Type: Pharmaceutical Company
Job Type: Pharmacovigilance
Job Level: Experienced (non manager)
Position: Full Time
Location: Cambridgeshire
Reference: NS78293
Closing Date: 29/06/20
Job Details:

Principal Pharmacovigilance Scientist


Location: Cambridge

Pharmaceutical Company

Salary: Lucrative, plus bonus and benefits

This global pharmaceutical client are looking for an experienced Senior PV Scientist to work closely with the Pharmacovigilance Physician and PV Scientist in order to author and lead the PV input into the safety documents and regulatory reports.

Responsibilities include:

  • Leading the meetings and presenting safety data and analyses
  • Lead and conduct proactive PV and Risk Management Plans and Risk Evaluation and Mitigation Strategies
  • Working with cross-functional project teams for development compounds and marketed products
  • You will lead and provide safety expertise to Investigator Brochures, Protocols, Informed Consents and Clinical Study Reports
  • Providing safety expertise to Investigator Brochures, Clinical Study Reports and Informed Consents
  • Leading data evaluation and collaboration with Clinical representatives
  • Authoring the Reference Safety Information for multiple complex development products
  • Authoring and providing strategic input and oversight for multiple periodic regulatory documents such as PBRERs, PSURs and DSURs
  • Training and mentoring junior members of the team


  • Life Science degree, MD, MSC or PhD preferred
  • Good understanding of PV regulations
  • Understanding of Epidemiology preferred
  • Ideally Post-marketing surveillance
  • Clinical Development experience (early or late phase)
  • Experience authoring RMPS and Periodic Reports is essential
  • Experience with Governance Board Interactions

To Apply

If you would like to discuss this vacancy further, please call i-Pharm Recruitment Consultant Niki Sansoy on +44 (0)20 3189 0470 or email


i-Pharm Consulting is a specialist Recruitment Company servicing the Pharmaceutical industry in the UK and Europe. 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.

Key Words: Pharmacovigilance/ Drug Safety /Pharma /PV/ UK/Cambridge/Hertfordshire/North London/Risk Management/Aggregatereports

Posted: 01/06/2020 | NPJ Ref: 254716
line graphic

Compatible with:

JobMate   Broadbean   Idibu

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

Credit cards image