Drug Safety Coordinator

• Excellent interepersonal communication skills, both written and oral
• Excellent computer skills in Microsoft environment (Microsoft Excel, Power point and Word)
• Safety database and data entry experience preferred
• Basic understanding of medical and drug terminology preferred
• Knowledge and experience with safety reporting and regulatory compliance and experience with international safety reporting/regulations is preferred
• Demontrates initiative, teamwork and accountability
• Demonstrated success working both independently and in collaboration with others
• A quality driven individual with strong attention to detail and accuracy is required
• Strong organizational skills, and ability to adapt to change
• A demonstrated ability to manage own workload, prioritize, plan and organize assignments and work under strick timelines is required
• Ability to follow guidelines and procedural documents Operations Sets work priorities and direction with input from Manager
• Review, extract and accurately enter AE data from ICSR reports from both investigational and postmarketing products
• Have solid working knowledge of protocol design and details relating to the extraction and entry of SAE from clinical trials reports
• Will have data review responsibility, to ensure data entries made by Safety Coordinators are accurate

All your information will be kept confidential according to EEO guidelines.