Description
Volt is recruiting on behalf of one of its leading Biotech clients in seeking a Drug Safety Specialist for a 12 months fixed-term contract. This is an excellent opportunity for an individual with some limited exposure to the pharmaceutical industry who is looking to progress their career within Pharmacovigilance.
Responsibilities:
-To manage safety data within the company's central safety database covering both pre and post market activities. To ensure compliance with internal case processing timelines. A regional role based in the UK.
-Ensuring that individual Adverse Event Case Reports are evaluated, investigated and accurately computerised
-Translation of source documents as needed
-Develop follow-up needs for AE reports and create follow-up letters, review and update generated follow-up letters as appropriate
-Support the identification of corrections and creation of updates in ARISg database following medical review
The successful candidate:
-Educated to BSc level in a Life Science related field, or a qualified Nurse or Pharmacist
-Some prior experience in the Pharmaceutical industry within Drug Safety, Medical Information, Regulatory Affairs or other related discipline
-Ideally has had some exposure to ARISg safety database and has experience in the therapeutic areas of haematology or oncology.
Volt is an established global recruitment business with an international presence spanning the IT, digital entertainment and pharmaceutical sectors. Volt Life Sciences recruits within biostatistics, clinical research, regulatory affairs, medical affairs, quality assurance, pharmacovigilance, market access and medical sales & marketing.