Beth Aherne Email & Phone Number

Wilmington, Delaware, US

Wilmington, Delaware, US

Wilmington, Delaware, US

Responsible for managing global operational teams and overseeing processes and functions for handling of adverse event/drug experience reports (serious and non-serious) and other safety related data for Incyte marketed products and clinical trials. Ensuring compliance with operational procedures and regulations for all Pharmacovigilance functions.

Wilmington, Delaware, US

Responsible for coordinating the timely completion and submission of required reports to health authorities and business partners. Assists with creating policies, SOPs, work instructions, forms and templates for efficient and effective processing of ICSRs. Responsible for the mentoring and personal development of direct reports. Ensures procedures are in.

Wilmington, Delaware, US

Reviews adverse drug experience reports entered into the Safety Database by a CRO. Responsible for reviewing narratives, follow-up requests, and coding of the adverse events in MedDRA in preparation for the finalization of the report as required. Ensures compliance with internal procedures, regulatory requirements and contractual requirements of Safety.

Wilmington, Delaware, US

Assists with the triage of events for expectedness and reportability along with the CRO and the drug safety associates. Assist with the receipt, assessment, tracking, follow-up, and regulatory reporting of adverse drug experiences received by Pharmacovigilance. Review adverse drug experience reports entered into the Safety Database by a CRO. Review the.

US

Responsible for collecting and processing adverse event reports for clinical trials, compassionate use trials, and marketed products. Assists in the development of safety surveillance processes and writing corresponding SOPs. Responsible for execution and management of literature searches for all ViroPharma products. Assists with safety database testing.

New York, New York, US

Responsibilities include processing and reviewing serious, non-serious individual case safety reports for investigational and marketed products, based on SOPs and regulatory guidelines. Assists with the preparation of Periodic Safety Reports, for transmittal to the FDA, WWRA and Business Partners.

Recruited for a project lead position conducting research in support of litigation for large pharmaceutical enterprises. Responsible for directing research projects including problem definition, research strategy and design, execution of research, analysis and presentation. Also responsible to complete projects under extreme deadlines, collaborate with.

Philadelphia, PA, US

• Provided nursing care on a 20-bed step down unit to critically ill children. Responsibilities included:
• Managing the care of 3-4 children per shift and coordinating patient care with an interdisciplinary team of doctors, nurses and other health care personnel.
• Also Responsible for the staffing and scheduling of approximately 40 nurses that worked on the unit.
• Charge nurse responsibilities included staffing of the unit, monitoring patient acuity changes and delegating instruction to the floor staff. Daily preparation as a charge nurse included working and communicating with.