This is an exciting opportunity for a Drug Safety Associate to join one of the leading international clinical research organisations (CROs).
You will be involved in reviewing SAE information from investigator sites and AEs from post marketing sources for completeness and regulatory compliance, as well as perform QC reviews of safety reports and preparing safety data reports for submissions to clients.
Because of the level of seniority of the position, you will be in contact with clinical operations personnel and clients to ensure compliance with safety and pharmacovigilance SOP as well as mentoring safety associates and other members of the safety and pharmacovigilance team.
Excellent training is provided and there is plenty of scope for development into more senior positions.
Who are we looking for? You will have a proven track record of working in drug safety and pharmacovigilance. A strong scientific or nursing background is essential for success in this role (equivalent experience will be considered).
For more information, please email Kristina at kristina@seltekconsultants.co.uk
Please note, that applying for this opportunity only expresses interest; we will discuss the role and company in detail with you before your CV is sent to the company.
Job Ref: 8083
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