6 Icsr Assessment Jobs

To lead a team of Drug Safety Physicians working on ICSRs Projects. Conduct initial assessment and Medical Review of ICSR s into the safety database. Review and verify appropriate selection of adverse events from source documents, check the seriousness criteria, appropriate MedDRA code, suspect drug, concomitant medications, lab data, medical history, labelling, causality, review narrative and provide Company Causality Comment. Review and respond to any queries/comments from the Case Owner in the Safety database. Train and mentor PV associates on event capturing and general PV conventions as required. Acquire and maintain current knowledge of product and safety profiles for products across t...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Performing triage and review for initial validity assessment of cases including spontaneous, health authority, Clinical Trial and literature cases. Data entry into PV database Initial ICSR assessment, if applicable Evaluation of the need for expedited reporting to Health Authorities / partners of a client c...

As a member of the team at Cencora, you will play a crucial role in creating healthier futures for people and animals everywhere. Your responsibilities will include: - Performing triage and review for initial validity assessment of cases, such as spontaneous, health authority, Clinical Trial, and literature cases. - Data entry into the PV database. - Conducting initial ICSR assessment, when applicable. - Evaluating the need for expedited reporting to Health Authorities or partners of a client, including reporting timelines. - Preparing standard reporting forms like CIOMS I/MedWatch Forms and XML files. - Sending follow-up requests and submitting ICSRs to Health Authorities and partners of a ...

As a valuable member of our team at Cencora, you play a crucial role in our mission to create healthier futures for all. Your dedication and contribution are key to our ability to deliver on this purpose. If you are passionate about making a positive impact on health, we invite you to join our dynamic company and work towards improving the well-being of people and animals worldwide. Take the first step today by applying for this exciting opportunity! Your responsibilities in this role will include: - Performing triage and reviewing cases for initial validity assessment, encompassing spontaneous, health authority, Clinical Trial, and literature cases. - Entering data into the Pharmacovigilanc...

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals everywhere. Apply today! Job Details Performing triage and review for initial validity assessment of cases including spontaneous, health authority, Clinical Trial and literature cases. Data entry into PV database Initial ICSR assessment, if applicable Evaluation of the need for expedited reporting to Health Authorities / partners of a client c...

As a valued member of our team at Cencora, you play a crucial role in our mission to create healthier futures for people and animals worldwide. Your contributions are essential to our ability to fulfill this purpose, and we invite you to be a part of our innovative company where you can make a real difference at the core of health. If you are passionate about improving lives and seeking a rewarding career, we encourage you to apply today. Your responsibilities will include: - Performing triage and review to assess the validity of cases, including spontaneous, health authority, Clinical Trial, and literature cases. - Entering data into the Pharmacovigilance (PV) database. - Conducting initial...