Pharmacovigilance Specialist

About the Role:We are seeking an experienced Pharmacovigilance Specialist to manage the collection, processing, and reporting of adverse event reports for our clients. The successful candidate will have expertise in pharmacovigilance and knowledge of national and international regulations.Key Responsibilities:Collect, process, and document adverse event...

We are seeking a highly skilled Pharmacovigilance Solutions Specialist to join our team at Industry Today. This role will focus on providing expert guidance on medical device regulations, ensuring compliance and operational excellence in the industry.Responsibilities:Develop and implement effective pharmacovigilance strategies for medical devicesCollaborate...

About the Role"We are seeking an experienced Pharmacovigilance Specialist to join our Clinical Safety team in London. As a key member of our team, you will be responsible for collecting, processing, and tracking SAE reports, generating safety narratives and queries, and performing quality control of safety cases."You will also prepare clinical safety...

Job Title: Pharmacovigilance Regulatory Compliance SpecialistWe are seeking a detail-oriented professional to administer our BI UK Pharmacovigilance system, ensuring 100% compliance with adverse event case processing, reporting timelines, and data quality.Key Responsibilities:Maintain accurate records of literature reviews, Malta legislation monitoring,...

As a Pharmacovigilance Business Growth Specialist, you will be responsible for developing and executing strategies to drive business growth through strategic partnerships. With a strong background in alliance management, partner development, or business growth, you will identify, recruit, and manage high-value partnerships that align with our business...

Job DescriptionThe Pharmacovigilance Writing Scientist will play a critical role in ensuring the effective delivery of business objectives within the Boehringer Ingelheim Pharmaceuticals, Inc. UK Pharmacovigilance system.This position is responsible for performing and maintaining areas of responsibility with the BI UK Pharmacovigilance system, focusing on...

Job DescriptionWe are looking for a highly skilled Senior Pharmacovigilance Compliance Specialist to join our team in the UK. The successful candidate will have experience in pharmacovigilance compliance, inspection, and audit readiness.Main Responsibilities:Ensure compliance with safety monitoring plans, study plans, metrics, KPIs, and contractual...

Overview:We are seeking a highly experienced Pharmacovigilance Senior Specialist to join our team in the UK. This is a 9-month temporary contract role that requires strong process development and maintenance skills.Job Description:As a Pharmacovigilance Senior Specialist, you will be responsible for contributing to the creation, maintenance, and archiving of...

Job DescriptionThis Global Pharmacovigilance Specialist role offers an exciting opportunity to contribute to the success of our clients by ensuring the highest level of safety standards in clinical trials. You will be responsible for managing SAE reports, generating safety narratives, and collaborating with cross-functional teams to ensure compliance and...

About RxLogix CorporationRxLogix is a leading provider of innovative pharmacovigilance solutions, empowering clients to enhance their drug safety capabilities.We foster collaborative relationships with Pharmacovigilance and Risk Management professionals to drive compliance, productivity, and quality improvements.Our commitment to patient safety and...

Job Title: Pharmacovigilance Specialist, Regulatory ReportingWe are seeking a skilled Pharmacovigilance Specialist to join our team at ProPharma Group. This role is responsible for ensuring adherence to daily operational processes within the Argus and ARISg database to guarantee adverse event submission compliance with health authorities, ethics committees,...

About Us:EPM Scientific is a leading provider of scientific expertise and services. Our team is dedicated to supporting the development and delivery of innovative healthcare solutions.Key Responsibilities:Process and code safety events using MedDRAEnter data into the Pharmacovigilance DatabaseMaintain the database and ensure accuracyMonitor adverse events...

About the RoleWe are seeking a skilled Pharmacovigilance Manager to join our team in Egham, UK.The successful candidate will be responsible for ensuring compliance with regulatory requirements and quality standards. They will work closely with the Head of Quality and Drug Safety to identify gaps in current processes and implement resolutions.Key...

About the RoleWe are seeking a skilled Pharmacovigilance Data Associate to join our team at EPM Scientific. As a key member of our safety team, you will be responsible for handling safety data, including adverse events, in compliance with regulatory requirements and company SOPs.Key Responsibilities:Assist in the processing of safety data, including MedDRA...

Job DescriptionThe estimated salary for this role is $110,000 - $140,000 per year.We are seeking a highly skilled Principal Pharmacovigilance Specialist to join our team at ProPharma. In this role, you will be responsible for providing directional leadership of PV clients and collaborating with Client Services on standard service offerings.As a subject...

At Medpace, our European Pharmacovigilance activities are rapidly growing. We are seeking motivated individuals to join our Clinical Safety team in London. This role plays a key part in accomplishing tasks and working on projects that contribute to the development of life-changing medicines.ResponsibilitiesWe collect, process, and track serious adverse event...

As a Pharmacovigilance Specialist, Submissions with ProPharma Group, you will be part of a team that improves the health and wellness of patients by providing advice and expertise to biotech, med device, and pharmaceutical organizations.The estimated salary for this role in London is around £55,000 - £70,000 per annum, depending on experience.Job...

About the Role:We are seeking a highly skilled Pharmacovigilance Specialist to join our team as an expert in case management. In this role, you will be responsible for providing oversight and direction as a PV subject matter expert, enhancing client service internally and externally.Key Responsibilities:Oversight and development of project/program specific...

About the RoleWe are seeking an exceptional individual to join our team as a Regulatory Affairs and Quality Assurance Specialist. As a key member of our regulatory and pharmacovigilance team, you will play a critical role in driving business growth and excellence through your expertise in regulatory affairs and quality assurance.This is a fantastic...

Veeva Systems, Inc. is a leading provider of industry cloud solutions for life sciences companies, helping them bring therapies to patients faster. With a strong mission-driven culture, the company is committed to making a positive impact on its customers, employees, and communities.We are seeking a highly skilled Senior Consultant – Safety & PV SME to...