Company: i-Pharm Consulting
Closing Date: 18 Jan 17
Salary (£): Negotiable
Pharmacovigilance Associate Manager - Major Biotech - 12+ Month Contracti-Pharm Consulting are seeking on behalf of a Leading Biotech a Pharmacovigilance Associate Manager to join their growing team in Cambridge.
Pharmacovigilance Associate Manager – Major Biotech – 12+ Month Contract
i-Pharm Consulting are seeking on behalf of a Leading Biotech a Pharmacovigilance Associate Manager to join their growing team in Cambridge.
Pharmacovigilance Associate Manager
Leading specialist Biotech with a global presence in over 100 countries. i-Pharm has been a dedicated recruiter for this client for a number of years and have had great feedback on the company’s career progression, culture and job satisfaction from candidates placed in both permanent and contract positions.
This is an excellent opportunity for a Drug Safety/Pharmacovigilance professional with strong experience in Signal Detection, Risk Management and writing PSURs. My client is offering a lengthy contract with scope for progression and further extensions along with an excellent hourly rate.
You will be involved in:
- Signal detection in collaboration with the safety physician
- Creation of aggregate safety reports (e.g., PSURs)
- Creation of risk management plans (RMPs)
- Authoring of responses to regulatory agency safety enquiries
- Input in safety analyses within Regulatory submissions
- Global literature review identifying potential safety concerns
- Contribution to safety committee meetings
- Signal detection
- Literature review
- Risk management
- Aggregate reporting (PSURs)
- Significant experience within the pharmaceutical industry
- Previous experience leading projects
- Educated to degree level or above, or professional qualification in a life science field
12+ Month Contract
Excellent Hourly Rate
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.
If you would like to discuss this vacancy further, please call Lauren McQuade on +44(0)2031890488, or email firstname.lastname@example.org. If this role is not suitable, Lauren is also available to discuss other possible positions or answer any general questions regarding your career and the current market.
Drug Safety / Clinical Safety / Pharmacovigilance / Drugs Safety / DrugSafety / PV / Regulatory / Pharmaceuticals / Pharmaceutical industry / Aggregate Reporting / Signal Detection / Literature Review / Risk Management / PSURs / CRO / Clinical Research Organisation / Pharma / ICSR / i-Pharm Consulting / i-Pharm London / Cambridge / Bedford / Peterborough / Bury St Edmonds
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