i-Pharm Consulting

Drug Safety Associate

Location
Windsor
Salary
Negotiable
Posted
27 Jul 2016
Closes
24 Jan 2019
Ref
NS2849
Contract Type
Permanent
Drug Safety Associate
Berkshire
Permanent
£Competitive with additional benefits

INTRO:
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.

RESPONSIBILITIES:

• 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

REQUIREMENTS:

• 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 nsansoy@i-pharmconsulting.com.
ABOUT i-PHARM CONSULTING

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

Similar jobs

Similar jobs