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Job Details
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Drug Safety Associate

Business Type: Pharmaceutical Company, Contract Research Organisation, Pharmaceutical Services
Job Type: Pharmacovigilance
Job Level: Experienced (non manager)
Position: Full Time
Location: United Kingdom
Reference: NS28495
Closing Date: 20/09/19
Job Details:

Drug Safety Associate
£Competitive with additional benefits

A growing CRO company are looking to expand the Pharmacovigilance team and therefore looking for an ambitious Drug Safety Associate with up to a year''s prior experience in industry. This company focus on both clinical and post marketed studies and have excellent relationships with the top pharmaceutical and biotechnology industries.


* Serious Adverse Events (SAE) reporting and processing
* Ensuring the safety database is set up for studies
* Coding SAEs
* Generating and reviewing reports used for Competent Authorities and Ethics Committee reporting
* Liaising with sponsors
* Data entry of SAEs
* Liaising with Data Managers to ensure SAE reconciliation
* Generating patient narratives
* Attends and presents on SAE reporting at Investigator meetings when required
* Attending client meetings


* Life sciences degree
* Prior experience working within Pharmacovigilance in either a CRO or pharmaceutical industry
* You must possess excellent communication skills
* Competent safety database user
* Excellent organisational skills
* Understanding of clinical trials methodology
* Prioritisation with workload and able to meet deadlines
* Working knowledge of ICH GCP and regulatory guidance
* Experience with data entry and interpretation of data
* Must have a working knowledge of coding dictionaries in pharmacovigilance
* Able to implement SOPs
* Must have practical IT skills
* Flexibility

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 / CRO / Pharma / UK

Posted: 23/08/2019 | NPJ Ref: 240740
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