Adverse Event Reporting Jobs in Raleigh, NC (NOW HIRING)

Promptly request all necessary medical records for Serious Adverse Event Reporting. * Process and ship laboratory biological samples for analysis. * Perform intraocular pressure checks after ...

Promptly request all necessary medical records for Serious Adverse Event Reporting. * Process and ship laboratory biological samples for analysis. * Perform intraocular pressure checks after ...

Manage the receipt and processing of all adverse event reports reported either spontaneously from any source or solicited from a clinical trial including safety database entry, AE review, write ...

Responsible for all tasks related to the collection, processing, follow up and regulatory reporting of adverse events (AEs), serious AEs from clinical trials (SAEs), adverse events of interest (AEIs ...

Provide the report to the conducting case owner * Identify, track, and file potential adverse event (AE) information. Additional responsibilities: * The Drug Safety Coordinator is the first person in ...

Implement quality control and assurance methods. * Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting.

Implement quality control and assurance methods. * Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting, protocol deviation reporting.

Communicate with study sponsors, research team and the Institutional Review Board. Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting ...

Communicate with study sponsors, research team and the Institutional Review Board. Assist with basic regulatory document preparation, with oversight e.g. study amendments, adverse event reporting ...

Ensure regulatory and study compliance by maintaining study documentation, regulatory binders, delegation of authority logs, adverse event reporting, and institutional and sponsor requirements.

Ensure regulatory and study compliance by maintaining study documentation, regulatory binders, delegation of authority logs, adverse event reporting, and institutional and sponsor requirements.

Key Responsibilities: ✔ Create and submit adverse event (AE) and product complaint (PC) reports ✔ Perform detailed quality control reviews for accuracy, spelling, manufacturer details, and ...

Assists the physician in completing and reporting state required adverse event reports and reporting internally as per organization/FMC policy and procedure. MAINTENANCE/TECHNICAL: * Operates ...

Confirms pharmacy department employees are trained on all required functions regarding payer and pharmaceutical contractual requirements (adverse event reporting, data and inventory reporting ...

Confirms pharmacy department employees are trained on all required functions regarding payer and pharmaceutical contractual requirements (adverse event reporting, data and inventory reporting ...

Confirms pharmacy department employees are trained in all required functions regarding payer and pharmaceutical contractual requirements (adverse event reporting, data and inventory reporting ...

Confirms pharmacy department employees are trained on all required functions regarding payer and pharmaceutical contractual requirements (adverse event reporting, data and inventory reporting ...

Oversight of adverse event processing by outsourced vendor, including the review and monitoring of compliance through various monitoring reports / KPIs;Participation in quality audits of individual ...

Independently prepare and submit regulatory documents including amendments, continuing reviews, adverse and serious adverse event reports within required reporting windows, and protocol deviation ...

Independently prepare and submit regulatory documents including amendments, continuing reviews, adverse and serious adverse event reports within required reporting windows, and protocol deviation ...