Pharmacovigilance Specialist

Job SummaryAs a Pharmacovigilance Specialist at Thermo Fisher Scientific, you will play a key role in ensuring the safety of our products and services. The ideal candidate will have a strong understanding of pharmacovigilance principles and practices, as well as excellent communication and problem-solving skills.Key ResponsibilitiesPerform day-to-day...

At Viatris, we empower people worldwide to live healthier at every stage of life. Our Pharmacovigilance team is crucial in ensuring the safety of our products, and we are seeking a skilled Pharmacovigilance Business Lead to join our team.The successful candidate will have a minimum of a bachelor's degree, preferably with a related health science or life...

Pharmacovigilance Associate Job DescriptionAt Engineeringuk, we're seeking a highly skilled Pharmacovigilance Associate to join our team. As a key member of our pharmacovigilance team, you will play a crucial role in ensuring the safety of our clients' products.Responsibilities:Review and process safety events, including pre-marketing, post-marketing,...

Job SummaryWe are seeking a highly skilled Pharmacovigilance Specialist or Safety Reporting Intelligence Expert to join our Pharmacovigilance Safety & Reporting group at ICON plc. As a key member of our team, you will be responsible for ensuring the timely and accurate processing of safety events, medical information call handling activities, and other...

Job Summary:We are seeking a highly skilled Pharmacovigilance Manager to join our team at ICON plc. As a key member of our Pharmacovigilance department, you will be responsible for managing personnel and providing expertise in various areas, including Serious Adverse Events (SAE) management, periodic safety reports, and regulatory compliance.Key...

Job Summary: We are seeking a skilled Pharmacovigilance Associate to join our team at ICON plc. As a Pharmacovigilance Associate, you will play a crucial role in ensuring the safety of our clients' products by reviewing and processing safety events, generating data listings, and performing adverse event follow-up.Key Responsibilities:Review and process...

At ICON plc, a world-leading healthcare intelligence and clinical research organization, we are seeking a highly skilled and experienced Senior Pharmacovigilance Manager to join our team.The successful candidate will be responsible for managing personnel within Pharmacovigilance and providing expertise in tasks such as Serious Adverse Events (SAE)...

At ICON plc, a world-leading healthcare intelligence and clinical research organization, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.Our mission is to accelerate the development of drugs and devices that save lives and improve quality of life, all...

About the RoleAs a Senior Pharmacovigilance Specialist at Thermo Fisher Scientific, you will play a critical role in ensuring the safety of new drugs in clinical trials and marketed products across all major markets. Your expertise in pharmacovigilance requirements will be essential in managing the safety profile of these products.Key...

Job DescriptionOverview:We are seeking a skilled Pharmacovigilance Specialist to join our team at Thermo Fisher Scientific. As a key member of our pharmacovigilance department, you will be responsible for performing day-to-day PV activities in a highly regulated environment.Responsibilities:Perform day-to-day PV activities, including data entry, coding, and...

About Johnson & JohnsonWe are a multinational healthcare company that has been transforming the history of health in humanity for over 130 years. With a mission to drive innovation and make a difference, we have impacted the lives of 1 billion patients daily.At Janssen, our approach is centered around fighting sickness with science, improving access with...

ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research by providing outsourced services to pharmaceutical, biotechnology, medical device, and government organizations.We put our patients at the center of everything we do, accelerating the development of drugs and devices...

We are seeking a highly skilled Pharmacovigilance Specialist to lead our team in collecting, monitoring, and assessing safety information in a highly regulated environment.Key Responsibilities:Oversee day-to-day pharmacovigilance activities and ensure quality, consistency, and accuracyParticipate in on-call duties for specific projects and provide expert...

At ICON plc, we are committed to advancing clinical research and providing high-quality services to our clients. As a Supervisor, Pharmacovigilance, you will play a critical role in supporting the creation and updates of SOPs, participating in departmental process and system improvement initiatives, and supervising a subordinated group.Key...

We are seeking a highly skilled Patient Safety Training Specialist to join our team at Novo Nordisk in Mexico City. As a key member of our Clinical, Medical & Regulatory department, you will play a vital role in ensuring the safety and efficacy of our products.**Job Overview**This is an exciting opportunity for a motivated professional with experience in...

Job OverviewAs a Senior Safety Data Specialist, you will play a key role in reviewing, assessing, and processing safety data and information across various service lines. This involves receiving data from multiple sources, analyzing it, and distributing reports to both internal and external stakeholders while adhering to applicable regulations and...

Patient Safety Training Specialist - GBS**Job Summary**Novo Nordisk is seeking a Patient Safety Training Specialist to join our Clinical, Medical & Regulatory department in Mexico City. As a Patient Safety Training Specialist, you will be responsible for planning, overseeing, coordinating, conducting, and documenting all Safety new hire training programs,...

As a Drug Safety Associate at Novo Nordisk, you will be responsible for performing initial evaluations, case entry, and verification of reported adverse events in the Argus safety database. This involves ensuring accurate coding of events using MedDRA and evaluating causality, seriousness, and listedness for all cases. You will also assess the need for...

Job OverviewAs a key member of our team, you will be responsible for reviewing, assessing, and processing safety data and information across various service lines. You will receive data from multiple sources and distribute reports and data to internal and external stakeholders in accordance with applicable regulations, Standard Operating Procedures (SOPs),...

About the RoleWe are seeking a highly skilled Safety Specialist II to join our team at Thermo Fisher Scientific. As a key member of our safety team, you will be responsible for managing the safety profile of new drugs in clinical trials, overseeing case-processing activities, and performing regulatory reporting and medical monitoring tasks.Key...