Drug Safety Associate

Drug safety associates have a wide range of responsibilities, which can include: - Reviewing adverse event reports, safety data sheets, and physician advisories to identify potential risks associated with a particular drug - Conducting site visits to observe the distribution process to ensure compliance with federal regulations - Monitoring compliance with...

Drug safety associates have a wide range of responsibilities, which can include: - Reviewing adverse event reports, safety data sheets, and physician advisories to identify potential risks associated with a particular drug - Conducting site visits to observe the distribution process to ensure compliance with federal regulations - Monitoring compliance with...

**Responsibilities for this position include**: - Identify out of scope activities in conjunction with the MSS Functional Lead - Determining the category of information received whether it is a Medical Inquiry, Product Quality Complaint (PQC), an adverse event (AE) associated with a PQC, or an AE alone, and handling it accordingly per the relevant SOPs and...

Review data entered in safety database for completeness and accuracy. - Provide quality feedback to team resources - Track and maintain quality metrics As Case Processor - Responsible for data entry of Individual case safety reports into the safety database. - Review and evaluate AE case information to determine required action based on and following...

**Job Summary** Responsible for providing medical and clinical insight and guidance through clinical trials for pharmaceuticals. **Primary Responsibilities** - Provide medical and clinical guidance to managers before, throughout, and following clinical trials. - Maintain consistency of safety assessments. - Perform a variety of safety assessments. - Serve...

Company DescriptionAt EVERSANA we are proud to be certified as a Great Place to Work across the globe We re fueled by our vision to create a healthier world How Our global team of more than 7 000 employees is committed to creating and delivering next-generation commercialization services to the life sciences industry We are grounded in our cultural...

Drug safety experts have numerous responsibilities and this can vary from one company to another. The roles include activities like. - Processing and writing of adverse event program - Follow up on important case reports - Serving as a link between company and the patients or healthcare experts to provide valid information on product safety. - Conducting...

Job Description:As a Senior Drug Safety Specialist, you will be responsible for collecting, tracking, and processing Adverse Events (AEs) from all sources with accuracy and efficiency. You will independently triage AEs to determine reportability in compliance with regulatory guidelines and clinical assessment standards.You will code AEs using MedDRA and...

A pharmacovigilance associate ensures compliance with applicable regulations or standard operating procedures; specialises in drug safety management, clinical trials and medical supervision. - Responsible for conducting, monitoring or reporting regular pharmacovigilance developments and supervising the processes related to ensuring drug effectiveness and...

As a Pharmacovigilance Associate you are part of the Pharmacovigilance Department (sometimes called the Drug Safety Department). Your role is one of reporting adverse effects (AEs) and side effects, in accordance with the current Dutch and European legislation for pharmacovigilance. You may also train colleagues in departments such as marketing and sales,...