Pharmacovigilance Jobs in Harrisburg
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Search Results - Pharmacovigilance Jobs in Harrisburg
GSK-Harrisburg
you will lead clinical safety and pharmacovigilance strategy for oncology assets within Global Safety.You will oversee rigorous review, interpretation and communication of safety data, ensuring timely identification, escalation and management of safety...
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GSK-Harrisburg
patients, evidence generation, regulators, payors, pharmacovigilance, etc.).Contribute to ambitious clinical development timelines by overseeing development of clinical study protocols, amendments, investigator brochures, clinical study reports etc.Input...
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GSK-Harrisburg
reflecting internal and external stakeholder input (e.g., patients, evidence generation, regulators, payors, pharmacovigilance).Bring clinical expertise to regulatory interactions and documents including briefing documents, presentations, addressing questions...
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GSK-Harrisburg
review of clinical trial data, both directly and through oversight of delegated medical review activitiesInterpret and contextualize safety data in collaboration with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefit–risk...
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GSK-Harrisburg
with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefit–risk assessment at the study level• Participate in safety review forums, including Safety Review Team (SRT) discussions, Independent Data Monitoring Committee (IDMC) data reviews...
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GSK-Harrisburg
with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefit–risk assessment at the study level• Participate in safety review forums, including Safety Review Team (SRT) discussions, Independent Data Monitoring Committee (IDMC) data reviews...
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GSK-Harrisburg
regulators, payors, pharmacovigilance), with an emphasis on early development.• Bring clinical expertise to regulatory interactions and documents including briefing documents, presentations, addressing questions and responses for assigned studies and programs...
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GSK-Harrisburg
review of clinical trial data, both directly and through oversight of delegated medical review activitiesInterpret and contextualize safety data in collaboration with pharmacovigilance, ensuring appropriate signal detection, escalation, and benefit–risk...
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GSK-Harrisburg
consistency and development of clinical capabilityDetailed Responsibilities:Medical Monitoring and Safety Oversightconsistency in approach, patient safety, and protocol adherenceGuide interpretation of safety data in collaboration with pharmacovigilance...
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GSK-Harrisburg
with other matrix Leads, such as the Global Regulatory Lead (GRL), the GML, etc. on oversight of clinical studies, patient safety & pharmacovigilance, scientific engagement and promotional practicesEnhance patient focus by incorporating the voice...
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GSK-Harrisburg
reflecting internal and external stakeholder input (e.g., patients, evidence generation, regulators, payors, pharmacovigilance).Bring clinical expertise to regulatory interactions and documents including briefing documents, presentations, addressing questions...
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GSK-Harrisburg
patient eligibility assessment, study design questions and medical data review.Review/monitor safety data in collaboration with pharmacovigilance group for active clinical studies.Participate in the authoring of clinical study reports and regulatory...
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GSK-Harrisburg
Products, Pharmacokinetics, Pharmacology, Pharmacovigilance, Target Research• If you are based in Cambridge, MA; Waltham, MA; Rockville, MD; or San Francisco, CA, the annual base salary for new hires in this position ranges $141,075 to $235,125.
The US...
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GSK-Harrisburg
interpretation of safety data in collaboration with pharmacovigilance, supporting signal detection, escalation, and benefit–risk evaluation across the programmeParticipate in and contribute to safety review forums (e.g., SRT, IDMC), providing senior physician...
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