Are you an experienced Senior PV Scientist? Do you have demonstrable experience with Safety Signals management?
You will be the product lead for Pharmacovigilance activities within our clients medical function.
Leads the signal management process (signal tracking) for assigned products and evaluates safety data and signals as part of ongoing pharmacovigilance activities.
Includes synthesis of data from multiple sources and authoring signal evaluation reports.
Collaborates with Global Safety Officers for assigned investigation programs including clinical trial activities protocol review, ICF review, safety committee management, data analysis, signal detection
Leads and collaborates with Aggregate Reports on strategy, review and finalisation of aggregate safety reports for assigned products, such as PSURs, DSURs, Pharmacovigilance Plans, Risk Evaluation and Mitigation Strategy Plans and Risk Management PlansExperience and skills:
Strong Pharmacovigilance experience
Experience in aggregate safety reports and safety signal management
Strong background in clinical trial drug safety is requiredThis is a PAYE Engagement contract. Rates negotiable depending on experience.
Randstad CPE values diversity and promotes equality. No terminology in this advert is intended to discriminate against any of the protected characteristics that fall under the Equality Act 2010. We encourage and welcome applications from all sections of society and are more than happy to discuss reasonable adjustments and/or additional arrangements as required to support your application.
Candidates must be eligible to live and work in the UK.
For the purposes of the Conduct Regulations 2003, when advertising permanent vacancies we are acting as an Employment Agency, and when advertising temporary/contract vacancies we are acting as an Employment Business