18 of 18 Remote Pharmacovigilance Jobs

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 More ❯

Integrity guidelines. Exploring Advanced Industry Systems: Work with and gain exposure to widely used systems, including ERPs , eDMS , eQMS , LIMS , laboratory systems, SCADAs , EBRs , pharmacovigilance, and maintenance systems. Assess system compliance with global standards to ensure efficiency and regulatory readiness. Auditing and Compliance Assessments: Perform audits of software suppliers to More ❯

other regulatory information management or submission publishing systems. 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 More ❯

top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy & Operations as well as Quality and Safety (eg. Pharmacovigilance). As a Consultant, you will manage workstreams on consulting projects for Veeva customers in R&D - planning, organizing, and tracking all aspects of delivery. More ❯

top 20 Pharmaceutical companies, to define and realize the strategic value of Regulatory Affairs, Clinical Strategy & Operations as well as Quality and Safety (eg. Pharmacovigilance). As a Senior Consultant, you will manage complex and novel consulting projects for Veeva customers in the research and development (R&D) space - managing More ❯

have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications More ❯

have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications More ❯

have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs/Writing. We are an equal opportunities Recruitment Business and Agency. We welcome applications More ❯

committed to making a positive impact on its customers, employees, and communities. The Role Help us transform and bring innovation to Drug Safety and Pharmacovigilance! Veeva is looking for an experienced consultant to join the Safety Professional Services team and support implementations of our Vault Safety solution. We want innovative More ❯

Sales Executive - Pharmacovigilance/Clinical Trial IT Solutions (Life Sciences) Full-Time, Hybrid Permanent Contract UK (St Neots/Hybrid/Homebased) Ennov is seeking sales representatives to strengthen its team in Europe. Reporting to our VP of Sales & Marketing in Paris, you will be responsible for selling our Pharmacovigilance … of life sciences organizations in a compliant and efficient way. With over 25 years of experience , Ennov's cloud-based solutions cover Regulatory Affairs, Pharmacovigilance, Quality, Clinical, and Document Management. Dedicated to innovation and excellence, Ennov's solutions are used by more than 450 Life Science companies and More ❯

committed to making a positive impact on its customers, employees, and communities. The Role Help us transform and bring innovation to Drug Safety and Pharmacovigilance! Veeva is looking for an experienced Senior Consultant to join the Safety Professional Services team and support implementations of our Vault Safety solution. We want … project team and junior consultants. Requirements At least 5 years of working experience in life sciences industry with the majority spent in Drug Safety, Pharmacovigilance, Healthcare, or adjacent Safety Industry. At least 3 years spent in a technology consulting role with solid experience in complex or global implementation projects as More ❯

from home or in the office, so you can thrive in your ideal environment. Help us transform and bring innovation to Drug Safety and Pharmacovigilance! Veeva is looking for senior system implementation experts with experience in PV Signal detection and analytics to join the Professional Services team and lead implementations … closely with the Product team and influence the design and features of our early adopter products Provide subject matter expertise on Drug Safety and Pharmacovigilance for customers and project teams Manage resources, lead and motivate a cross-functional team, and track and forecast projects Act as primary contact for customer … presales/sales teams in defining scope, costs, and estimations Requirements 5+ years of experience in the life sciences industry, especially in Drug Safety, Pharmacovigilance, Healthcare, or related Safety fields Subject matter expertise in Signal Detection Experience with safety databases like ARISg (LifeSphere), ARGUS, Empirica, or similar PV solutions Self More ❯

Reporting directly to the Head of PV and Medical Director, we are seeking a skilled Pharmacovigilance Systems Programmer experienced in PV and medical systems (e.g. Argus, Veeva, HaloPV, etc) with expertise in coding (e.g. SQL), systems programming, configurations, validation, report and dashboards development, ideally with a background in pharmacovigilance (PV … and medical services systems at TMC. The ideal candidate will have experience using industry-standard databases, appropriate programming expertise and a working knowledge of pharmacovigilance processes in the EU, US, and/or UK markets. They will play a key role in ensuring seamless database migrations, implementation and personalization for … IN HARTLEY WINTNEY IN HAMPSHIRE, U K Key Responsibilities Manage the transition and setup of the existing Argus safety database to Halo PV, a pharmacovigilance safety databases and ensure regulatory compliance. Develop, maintain, and optimize SQL queries to support pharmacovigilance and medical information systems. Configure and maintain Veeva for medical More ❯

expertise to connect life science companies, public health, and regulatory sectors to the right safety solutions. we take pride in being the leading specialist pharmacovigilance provider, offering unparalleled expertise in PV services, technology, and consulting to cater to the unique needs of small, medium, and large pharmaceutical companies. Job Title … Croatia or India Job Type: Full-Time Job Description: We are seeking a Consulting Technology Project Manager to manage client implementation projects for our Pharmacovigilance SaaS solutions. The ideal candidate will be a dynamic client facing services professional with extensive project management experience in the life science technology domain. This … project documentation, including project initiation documents, risk management plans, and post-project reviews. Ensure all projects comply with industry regulations, particularly those related to pharmacovigilance and data privacy (e.g. GxP, GDPR). Coordinate and manage interactions with third-party vendors, consultants, and partners to ensure successful delivery and integration of More ❯

Cambridge, MA POSITION : Lead Report Developer POSITION DESCRIPTION : Takeda Development Center Americas, Inc. is seeking a Lead Report Developer with the following duties: Deliver pharmacovigilance (PV) reporting & analytic solutions for Takeda Patient Safety & Pharmacovigilance (PSPV); Identify and develop methods for statistics and AI/Machine Learning to support the department … s data needs; Solve business problems in drug safety which provide an increased understanding of such tools and techniques. Identify and document Global Pharmacovigilance reporting end-user system needs and requirements; Provide strategic technical input into development of roadmaps and plans for implementing Business Intelligence (BI) capabilities (reporting, interactive analysis … views, dashboards, etc.) in response to global pharmacovigilance user requirements and/or regulatory guidance; Lead and perform user needs and requirements analysis, support construction and maintenance of BI solutions, using Oracle, Cognos, and other applicable technologies, which include definition of requirements, designs, source code development, unit testing, maintenance, and More ❯

our team as the Associate Director, PV Systems Application Development. This pivotal role acts as a key liaison between stakeholders and end-users of Pharmacovigilance (PV) computer systems, and IT service providers, ensuring seamless systems delivery, validation, and support. The successful candidate will demonstrate expertise in project management, business and … Bachelor's degree (BS/BA) in a scientific or medically related field, or equivalent experience in the pharmaceutical industry, specifically in clinical development, pharmacovigilance, and information management. Experience managing safety databases. Comprehensive understanding of pharmacovigilance (PV) and drug safety system lifecycle management. In-depth knowledge of clinical safety and … pharmacovigilance data, processes, and regulations. Thorough knowledge of database management, and systems analysis and design. Preferred Qualifications & Skills: Please note the following skills are not necessary, just preferred. If you do not have them, please still apply: Proficiency with ARGUS safety database. Strong background in information management. Thorough knowledge of More ❯

sales representatives to strengthen its team in Europe. Reporting to our VP of Sales & Marketing in Paris, you will be responsible for selling our Pharmacovigilance and Clinical Trials solutions to clients in the life sciences and healthcare sectors located in Europe, and potentially in Asia. Possibility for full remote in … of life sciences organizations in a compliant and efficient way. With over 25 years of experience , Ennov's cloud-based solutions cover Regulatory Affairs, Pharmacovigilance, Quality, Clinical, and Document Management. Dedicated to innovation and excellence, Ennov's solutions are used by more than 450 Life Science companies and More ❯

Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l'international, l'anglais étant la langue de travail. This job offer is accessible to all, regardless of gender. Job title : Data More ❯