i-Pharm Consulting

Principal Drug Safety Associate

06 Nov 2018
19 Dec 2018
Contract Type
Principal Drug Safety Associate
Europe- office based
Company- CRO

Salary: £Negotiable with discretionary bonus


A fantastic opportunity has arisen for an experienced Principal Drug Safety Associate to a join a top global CRO. The suitable candidate will have strong PV project management experience and must have previous client facing experience in industry.

This company have a well-established global presence and work with the top pharmaceutical, biotechnology and medical device companies to deliver high quality service within all phases of clinical trials. The working environment within the department is sociable and warming which makes for a great working atmosphere!


* Co-ordinating and performing AE data and case assessment, review and follow up
* Mentoring and training junior members of staff
* Participation in candidate interviews
* Interface with project team members and client contacts
* Serving as a Project Lead
* Involvement in routine project implementation and coordination, i.e presentations at investigator meetings
* Review of metrics and budgets


* Bachelors in Life Science Subject
* Strong knowledge of case processing experience- predominately within clinical trials
* Ideally previous CRO experience although not mandatory
* Experience with oversight of team and managing deliverables
* Ideally financial experience
* Line management experience is ideal
* Good PV systems knowledge
* Project management experience, as well as interacting with stakeholders (internal or external)

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 nsansoy@i-pharmconsulting.com.

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 / CRO / Pharma / UK/Senior/Principal

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