Pharmacovigilance Expert

Job Title: Pharmacovigilance ExpertCompany Overview:Russell Tobin is a leading pharmaceutical company committed to delivering innovative solutions for patients worldwide.Job Summary:The Pharmacovigilance Expert will play a vital role in ensuring compliance with pharmacovigilance regulations and guidelines while managing adverse event reports for various...

Job Title: Pharmacovigilance ExpertLocation: London, UKEstimated Salary: £80,000 - £110,000 per annumJob Description:We are seeking an experienced Pharmacovigilance Expert to join our team at GlaxoSmithKline. As a key member of our safety risk management team, you will be responsible for detecting and evaluating signals related to our products.Key...

Job DescriptionWe are seeking a highly skilled Pharmacovigilance Expert to join our team at GlaxoSmithKline in London, UK. As a key member of our pharmacovigilance team, you will be responsible for providing in-depth medical/scientific expertise in the safety evaluation and risk management of our products.

About UsGlaxoSmithKline is a global biopharmaceutical company dedicated to improving human health. We have a long history of innovation and are committed to making a positive impact on society.We offer a competitive salary range of $120,000 - $160,000 per annum, depending on location and experience.Job DescriptionWe are seeking a Pharmacovigilance Leadership...

Job DescriptionWe are seeking a highly skilled Pharmacovigilance Expert to join our team at ProPharma. This is an exciting opportunity for a seasoned professional to take on a challenging role in Case Processing. In this position, you will be responsible for leading the development of detailed project/program specific documents, such as Working Practices,...

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...

**Role Summary:**We are seeking a highly skilled Data Safety Expert - Pharmacovigilance to join our team in London. As a key member of the safety team, you will be responsible for ensuring the safe and effective handling of safety data, including adverse events, in compliance with regulatory requirements and company SOPs.**Key Responsibilities:**Case...

Job OpportunityWe are seeking a skilled Content Writer to join our dynamic team at BioTalent. This hybrid role based in London offers an exciting opportunity for creative professionals to craft compelling content that resonates with global audiences within the pharmacovigilance and drug safety space.Key Responsibilities:Develop high-quality content for web,...

About the Role:This role is a critical part of our team, responsible for ensuring the safety and efficacy of our products. As a Global Pharmacovigilance Expert, you will lead the development and implementation of strategies to evaluate and manage safety risks associated with our products.

Job OverviewThe Pharmacovigilance Writing Scientist will play a crucial role in ensuring the effective delivery of business objectives within the BI UK Pharmacovigilance system. This includes maintaining 100% compliance with adverse event case processing, reporting timelines, and data quality.

ResponsibilitiesThis challenging role involves establishing and maintaining local PV systems, providing strategic leadership and guidance to Pharmacovigilance (PV) and Medical Information (MI) team members, and overseeing all local pharmacovigilance activities. You will be responsible for managing Individual Case Safety Reports (ICSRs), reconciling ICSRs...

About the Role: As a Safety Data Expert, you will be responsible for leading pharmacovigilance compliance, inspection, and audit readiness for Argus, KPIs, and safety management topics. You will oversee ICSR workflow, case management activities in Argus and provide pharmacovigilance oversight for clinical trials, post-market surveillance, and expanded access...

We are looking for a highly skilled Medical Science Expert - Pharmacovigilance to join our team at GlaxoSmithKline.">The successful candidate will be responsible for leading the safety component of global regulatory submissions and developing strategy for approach to evaluation of issues in the clinical matrix.">They will have expert evaluation skills and...

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 RoleWe are seeking a highly skilled Medical Doctor or equivalent to join our team as a Safety and Risk Management Professional. The ideal candidate will have substantial experience in pharmacovigilance and drug development, with a strong understanding of international pharmacovigilance requirements and drug approval processes.The successful...

**About the Role:**We are seeking a highly experienced Pharmacovigilance Operations Manager to join our team at EPM Scientific. As a key member of our pharmacovigilance department, you will be responsible for ensuring compliance with regulations and quality standards across all processes.The ideal candidate will have a strong background in pharmacovigilance,...

About Veeva SystemsVeeva Systems is a mission-driven organization that has revolutionized the industry cloud, enabling life sciences companies to accelerate therapy delivery to patients faster.As a pioneer in this field, Veeva has made a significant impact on customers, employees, and communities, solidifying its position as a leader in the life sciences...

Job Overview:The successful candidate will be responsible for administering our BI UK Pharmacovigilance system, ensuring compliance with regulatory requirements and maintaining accurate records.Key Responsibilities:Ensure 100% compliance with adverse event case processing, reporting timelines, and data quality.Maintain accurate and up-to-date records of...

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...

**Job Description:**EPM Scientific, a global specialty pharmaceutical group, is seeking an experienced Pharmacovigilance Associate Professional to join their team in London. This role offers a unique opportunity to work with world-leading scientific experts and contribute to the development of treatments for patients with genetic, metabolic, systemic, and...