Hourly Adverse Event Reporting Jobs (NOW HIRING)

Support Medical Device Report (MDR) activities. Review and process complaint records. Manage adverse event reporting. Monitor medical device surveillance. Maintain MDR and ADE records. Review ...

Support the preparation, review, and submission of adverse event reports to regulatory authorities as required. * Collaborate with Quality, Regulatory Affairs, Medical Affairs, Clinical Affairs ...

Support the preparation, review, and submission of adverse event reports to regulatory authorities as required. * Collaborate with Quality, Regulatory Affairs, Medical Affairs, Clinical Affairs ...

Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...

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 ...

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 ...

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

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

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

At Hologic, we are seeking a Clinical QA Specialist to play a critical role in the investigation and reporting of potential and actual adverse events, as well as other regulatory reporting activities.

Job Summary The Adverse Event Specialist is responsible for both product complaint remediation and ... It ensures that all MDR submissions are completed in full compliance with FDA reporting ...

Implement protocols, processes, procedures, and tracking systems for adverse event reporting systems, statistical summaries, and data requests. Under supervision of program staff, review and respond ...

Review product complaints and adverse event reports to assess reportability and determine whether device use contributed to patient harm. * Interface with customers to collect patient information and ...

Implement protocols, processes, procedures, and tracking systems for adverse event reporting systems, statistical summaries, and data requests. Under supervision of program staff, review and respond ...

Enter adverse event reports into the tracking log, determine whether they are initial, follow-up, or duplicate reports, and create appropriate case folders. * Review source documents to identify and ...

Also engages in adverse event reporting, product quality complaint reporting, and other processes as required. Completes special assignments. Interacts with business partners external to the MIC.

Implement protocols, processes, procedures, and tracking systems for adverse event reporting systems, statistical summaries, and data requests. Under supervision of program staff, review and respond ...

Implement protocols, processes, procedures, and tracking systems for adverse event reporting systems, statistical summaries, and data requests. Under supervision of program staff, review and respond ...