Manager Adverse Event Reporting Jobs (NOW HIRING)

Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...

Responsibilities involve patient registration, data management, adverse event reporting, maintenance of a Clinical Trials Management System, and other activities related to research. The RDS works ...

Risk Managers will also be considered. * 5+ years of experience in a similar role, preferably within the medical device or healthcare industry. * Hands-on experience with adverse event reporting ...

Risk Managers will also be considered. * 5+ years of experience in a similar role, preferably within the medical device or healthcare industry. * Hands-on experience with adverse event reporting ...

Advocates manage complex documentation, medication ordering, adverse event reporting, and client-specific processes while providing empathetic, high-quality customer service. The position requires ...

Receives and reviews adverse event reports (computerized + phone) * Manages intake and ensures timely follow-up * Identifies sentinel events (SREs) * Provides initial response guidance to staff

Receives and reviews adverse event reports (computerized + phone) * Manages intake and ensures timely follow-up * Identifies sentinel events (SREs) * Provides initial response guidance to staff

Advocates manage complex documentation, medication ordering, adverse event reporting, and client-specific processes while providing empathetic, high-quality customer service. The position requires ...

Manage clinical trial operations from startup through closeout Oversee adverse event reporting and pharmacovigilance systems Ensure compliance with ICH-GCP and regulatory requirements Coordinate DSMB ...

Advocates manage complex documentation, medication ordering, adverse event reporting, and client-specific processes while providing empathetic, high-quality customer service. The position requires ...

Advocates manage complex documentation, medication ordering, adverse event reporting, and client-specific processes while providing empathetic, high-quality customer service. The position requires ...

Requirements Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH ...

Provides medical evaluation of adverse event reports * Performs various tasks in support of clinical research including the reporting, collecting, and sharing of results and issues around adverse ...

Key Responsibilities: • Manage clinical trial operations from startup through closeout • Oversee adverse event reporting and pharmacovigilance systems • Ensure compliance with ICH-GCP and ...

Ensures compliance with TRI Standard Operating Procedures, Food and Drug Administration and World Health Organization regulations and global regulations for the reporting of adverse events to ...

Experience managing investigations, adverse event reporting, and regulatory documentation * Hands-on experience with regulatory databases/platforms and compliance systems * Background supporting ...

... complaint handling, adverse event reporting, MDR evaluation, post-market surveillance, or ... management systems such as SAP, TrackWise, or similar platforms The Company offers the following ...

Adverse event reporting and monitoring * Tort claim processing * Death and disability case reviews ... Data Management & Reporting * Provide guidance on database management and data analysis. * Prepare ...

The Clinical Risk Manager will be responsible for clinical aspects of risk management and will be ... Prepares clinical case reviews for adverse event reporting to excess carrier and primary ...

Adverse event reporting and monitoring * Tort claim processing * Death and disability case reviews ... Data Management & Reporting * Provide guidance on database management and data analysis. * Prepare ...