Job Details

Pharmacovigilance Officer – Cambridgeshire

An interesting opportunity to gain diverse experience has arisen for a Pharmacovigilance Surveillance Scientist with vast industry experience. The company itself is dedicated to the research and development of highly effective and innovative medications have successfully generated an environment in which employees are able to commit themselves to their work whilst developing and contributing their specialist knowledge. This is an excellent opportunity to take on a contract for 9 months

Pharmacovigilance Officer – New Contract - Cambridgeshire An interesting opportunity to gain diverse experience has arisen for a Pharmacovigilance Surveillance Scientist with vast industry experience. The company itself is dedicated to the research and development of highly effective and innovative medications have successfully generated an environment in which employees are able to commit themselves to their work whilst developing and contributing their specialist knowledge. This is an excellent opportunity to take on a contract for 9 months and work closely in a strong and close knit environment. As Pharmacovigilance Officer your responsibilities will include: Timely processing of adverse event reports from clinical studies, post-marketing studies, spontaneous, regulatory authority and literature report sources in compliance with regulatory obligations o Involving tracking, data entrycase assessment, narrative writing o Quality check o Preparation and submission of expedited reports to regulatory authorities according to local timelines o Obtain timely follow up information from patients and healthcare professionals o Transmission of electronic reports to European Authorities as appropriate Perform reconciliation procedures with other departments or companies to monitor and ensure that all adverse event reports have been received and appropriately processed Work closely with the Independent Associated Companies to allow timely submission of adverse event reports to European Drug Safety and Pharmacovigilance for data processing Keep up-to-date with Pharmacovigilance Guidelines and Directives Review and update departmental SOPs and Administrative Guidelines as required Successful applicants will have strong pharmacovigilance experience within the industry. This is an excellent opportunity for someone with great organisational skills and attention to detail to be part of a hardworking and enthusiastic team. For a confidential discussion and to find out more information about this role please contact Harriet Maidman on 0207 234 0550 or by e-mail to h.maidman@nonstop-pharma.com NonStop Recruitment are committed to best practice, we abide by the Conduct of Employment Agencies and Employment Businesses Regulations 2003; we are Recruitment and Employment Confederation (REC) members and follow the REC Code of Professional Practice and Code of Ethics 2003.