Pharmacovigilance Specialist

Job OverviewBristol Myers Squibb is a leading pharmaceutical company dedicated to transforming patients' lives through science. We are seeking an experienced Senior Pharmacovigilance Specialist to join our team.About the RoleWe offer a competitive salary of $120,000 per annum, plus benefits. As a Senior Pharmacovigilance Specialist, you will be responsible...

Key ResponsibilitiesAs a Senior Pharmacovigilance Compliance Specialist at Bristol Myers Squibb, you will be responsible for ensuring the safety of our medicines by ensuring compliance with global regulatory requirements. You will have a strong scientific background in a life science related field and 5 years of pharmaceutical industry experience, including...

Job SummaryWe are seeking a highly skilled Quality Assurance Specialist, Pharmacovigilance to join our team at Bristol Myers Squibb. The successful candidate will be responsible for ensuring the quality and compliance of our pharmacovigilance activities, including safety database case processing, quality monitoring, and compliance with global regulatory...

Job SummaryWe are seeking a highly skilled Senior Pharmacovigilance Compliance Specialist to join our team at Bristol Myers Squibb. As a key member of our Worldwide Patient Safety group, you will be responsible for ensuring the safety of our medicines and ensuring compliance with global regulatory requirements.Key ResponsibilitiesProvide quality oversight...

Job SummaryThe Senior Pharmacovigilance Compliance Specialist will be responsible for ensuring the safety of our medicines by ensuring compliance with global regulatory requirements. This includes monitoring safety outputs to ensure quality excellence and compliance with worldwide GVP regulations, guidance, and inspectorate expectations.Key...

Job SummaryWe are seeking a highly skilled Pharmacovigilance Quality Assurance Specialist to join our team at Bristol Myers Squibb. In this role, you will be responsible for ensuring the quality and compliance of our pharmacovigilance activities, including safety database case processing and quality monitoring.Key ResponsibilitiesPerform ongoing monitoring...

Company OverviewPharma Stuff, a leading pharmaceutical manufacturing company, is dedicated to innovation and quality in the production of life-saving drugs. With a strong presence in the Pharmaceutical Manufacturing industry, our firm employs over 1000 professionals focused on excellence. We promote growth by nurturing talented individuals from within our...

Job SummaryAs a Quality Assurance Specialist at Bristol Myers Squibb, you will be responsible for ensuring the quality and compliance of our pharmacovigilance activities. This includes monitoring safety outputs, ensuring compliance with global regulations, and implementing quality improvement initiatives.Key ResponsibilitiesPerform ongoing monitoring of...

Job SummaryWe are seeking a highly skilled PV Compliance Specialist to join our team at Bristol Myers Squibb. As a PV Compliance Specialist, you will be responsible for ensuring the safety of our medicines by monitoring safety outputs and ensuring compliance with global regulatory requirements.Key ResponsibilitiesProvide compliance oversight through ongoing...

Job Title: PV Compliance and Quality Risk Management SpecialistThe Worldwide Patient Safety (WWPS) group is responsible for ensuring the safety of our medicines through pharmacovigilance and pharmaco-epidemiology deliverables. This includes single case and aggregate safety monitoring, safety reporting, contribution to benefit-risk assessment, risk management...

Job SummaryWe are seeking a highly skilled PV Compliance Specialist to join our team at Bristol Myers Squibb. This individual will be responsible for ensuring compliance with global regulatory requirements and ensuring the quality and safety of our medicines.Key ResponsibilitiesProvide compliance oversight through ongoing monitoring of safety outputs created...

Job SummaryAt Bristol Myers Squibb, we are seeking a highly skilled Learning Media and Communication Specialist to join our team. As a key member of our Pharmacovigilance and Risk Management (PV PELS) team, you will play a pivotal role in optimizing and analyzing the effectiveness of media assets used in training and communications materials.Key...

At Lifelancer, we're looking for a seasoned professional to join our team as a Global Medical Specialist. This role is perfect for individuals with a strong background in medical affairs, clinical development, and pharmacovigilance.About the JobWe're seeking an expert with at least 5 years of experience supporting international pharmaceutical companies. Your...

About the Role:We are seeking a skilled Medical Review Specialist - Pharmacovigilance to join our team at Parexel.Responsibilities:Perform medical review of cases according to client Standard Operating Procedures (SOPs) and liaise with the client, as required.Write Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assess company...

About the RoleThis position plays a vital role in ensuring compliance with global regulatory requirements and pharmacovigilance guidelines. As a Manager of Regulatory Compliance, you will oversee quality, compliance, and inspection readiness activities within the Worldwide Patient Safety group.Key ResponsibilitiesOversight of compliance monitoring programs...

Job SummaryWe are seeking a highly skilled Pharmacovigilance Quality Risk Manager to join our team at Bristol Myers Squibb. As a key member of our Worldwide Patient Safety group, you will be responsible for ensuring the safety of our medicines through ongoing monitoring of safety outputs and compliance with global regulatory requirements.Key...

Job Summary:Parexel is seeking a highly skilled Senior Drug Safety Physician to join our team. As a key member of our Pharmacovigilance department, you will be responsible for providing medical review, analysis, and guidance during the case handling and reporting cycle of Adverse Event and Adverse Reaction reports received for investigational and marketed...

Job SummaryThe ideal candidate will possess a strong background in pharmacovigilance and safety data processing, with a focus on adverse event reconciliation. In this role, the Safety Data Analyst, Reconciliation Specialist will be responsible for reviewing and reconciling adverse event data in the Worldwide Patient Safety database and clinical trial...

About the RoleThe Worldwide Patient Safety group at Bristol Myers Squibb is responsible for ensuring the safety of our medicines. As a Safety Specialist, Regulatory Compliance, you will contribute to pharmacovigilance and pharmaco-epidemiology deliverables, including single case and aggregate safety monitoring, safety reporting, and risk management...

Job SummaryThe Learning Media and Communication Specialist will play a pivotal role in the PV PELS and broader WWPS team, focusing on optimizing and analyzing the effectiveness of media assets used in training and communications materials. This role aims to enhance the learning experience by evaluating and implementing various media elements, ensuring...