of software and service solutions and adapt current solutions, to create new & improved client centric offerings Identify and respond to customer needs to define potential opportunities for Regulatory/Pharmacovigilance solutions and propose appropriate tailored solution in line with client needs Manage assigned strategic and key account relationships individually or in coordination with Global and Regional Sales Teams Requirements Must … volume and high velocity sales organization Bachelor's degree or equivalent experience required Willing to travel as needed throughout EMEA area Highly preferred capabilities: Possess an understanding of the pharmacovigilance process for both pre-marketed and post-marketed stages of a product Selling drug safety and regulatory consulting services, hosting, managed services, and products Experience working with Heads of Safety More ❯
Manager, Master Control, Trackwise, other regulatory information management or submission publishing systems, etc. Consulting experience, working with a major system integrator or software vendor Regulatory Affairs, Regulatory Operations or Pharmacovigilance background Knowledge of Pharmaceutical, Biotechnology, and/or Medical Device and Diagnostics regulatory processes, data and content PMP certification Execution experience with Agile methodology and/or ACP Certification Life More ❯
weeks ago Senior Manager Strategy & Operations - Technology London, England, United Kingdom 1 week ago Sr. Program Manager, Executive Selling Partner Relations London, England, United Kingdom 1 week ago Senior Pharmacovigilance Manager, Case Processing Director/Senior Director - Consulting (HEOR + HTA) London, England, United Kingdom 1 week ago Italian- Customer Success Manager: Program Specialist London, England, United Kingdom 2 weeks More ❯
Candidates must be located in UK (preferably London)** Company Overview: RxLogix is a global leader in pharmacovigilance solutions, providing innovative software and expert consulting services. Our team collaborates with Pharmacovigilance and Risk Management professionals to enhance compliance, productivity, and quality across the drug safety value chain. Dedicated to patient safety and the advancement of medical and scientific research, RxLogix values … along with a track record of successfully selling enterprise software solutions (preferably SaaS). Previous experience selling into the pharmaceutical and CRO industry is preferred. Previous experience with selling Pharmacovigilance and Drug Safety Software. Previous experience presenting online to a wide variety of clients, including senior level executives, and proven success closing the sale. Ability to stand up in front More ❯
This post is only open to internal applicants. Research & Development (R&D) Systems Lead NHS AfC: Band 8a Main area Research & Development Grade NHS AfC: Band 8a Contract Permanent Hours Full time - 37.5 hours per week Job ref 213-CORP More ❯
proven experience in the pharmaceutical or healthcare industry. Backgrounds in Quality Assurance, Clinical Development, or supervised IT support are all highly relevant. Familiarity with Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), and the software development lifecycle for validated systems is required. Veeva Vault experience is strongly preferred. Experience generating quality reports, handling upgrades, or serving as a subject matter More ❯
medicines, including in silico modelling to enhance safety evaluations. Biological safety, and sterilisation and decontamination assessment: underpinning both post-market surveillance and clinical investigations for medical devices. Pharmacogenomics for pharmacovigilance: co-ordinate policy on the integration of pharmacogenomics with pharmacovigilance to support personalised medicine, ensuring our approach remains at the forefront of healthcare. Emerging technologies: lead policy on post-market More ❯
provide scientific and commercial expertise, defining new service offerings that will create a competitive advantage. Reporting to the Head of the Late Phase business unit, your expertise will include: Pharmacovigilance and Safety Observational studies and Patient Registries Interventional studies HEOR Real world evidence Managed/Expanded access programs As Vice President, Subject Matter Expert, Late Phase you will be expected More ❯
