1 to 25 of 27 Pharmacovigilance Jobs in the UK

the following areas - R&D strategy and operating model; pipeline/portfolio/asset strategy; product launch; digital transformation and innovation; clinical, regulatory and pharmacovigilance; data, analytics and AI; patient and investigator experience Exceptional creative problem solving and analytical skills Team leadership experience Business development experience Effective communication skills, both More ❯

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 ❯

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 ❯

Chief Medical Officer. These solutions span the entire clinical development lifecycle, including protocol development, patient-centric approaches, clinical trial design and execution, regulatory submissions, pharmacovigilance and others. By harnessing cutting-edge technology, data, and analytics, we enable operational excellence, ensure regulatory compliance, and drive impactful decision-making to accelerate the 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 ❯

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 ❯

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 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 ❯

Oversee the management of investigator-initiated trials, ensuring systems are established to monitor all aspects of study progress, including screening, recruitment, compliance, IMP management, pharmacovigilance and reporting. Oversee the development and use of electronic regulatory documentation and digital pharmacovigilance systems to enhance reporting accuracy and compliance Prepare or oversee preparation … relevant scientists Managerial, Supervisory, Advisory Responsibilities Structure the DDU-IIT team with appropriate workforce planning and securing appropriate funding. Supervise all project management, monitoring, pharmacovigilance and data management activities undertaken within the DDU-IIT team. Oversee staff recruitment and development including objective setting, performance appraisal and training. Remain directly responsible 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 ❯

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 … 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 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 ❯

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 ❯

Director, Global PV Systems Configuration Management Are you energized by the opportunity to work with global stakeholders to design and support critical, highly visible Pharmacovigilance Systems Configuration that have a global impact? If so, this role could be an ideal opportunity for you. The PV Systems group enables Global Safety … to be ambitious for patients by linking Pharmacovigilance (PV) system users and Digital and Tech in key areas including systems delivery, configuration, validation, and support. The key activities include: Project Management Business Analysis Data Analysis Systems Validation Systems Support, Configuration, and Maintenance Training The Director manages one of the three … BS/BA in a relevant scientific, life sciences, or medical field or equivalent experience. 10+ years in the pharmaceutical industry, including clinical development, pharmacovigilance, and information management. Experience with database management, systems analysis, design, and drug safety systems. Experience in configuration management in safety databases, with logical operational mapping More ❯

Director, Global PV Systems Configuration Management Are you energized by the opportunity to work with global stakeholders to design and support critical highly visible Pharmacovigilance Systems Configuration that have a global impact? If so, this Director, Global PV Systems Configuration Management role could be an ideal opportunity to explore. The … PV Systems group enables Global Safety to be ambitious for patients by linking Pharmacovigilance (PV) system users and Digital and Tech several key areas including - systems delivery and configuration, systems validation, and systems support. The key systems management activities include: Project Management Business Analysis Data Analysis Systems Validation Systems Support … Global Safety • Proactively identify areas which would benefit from new systems and technology by maintaining awareness of industry trends and regulatory changes worldwide in pharmacovigilance • Lead delivery of innovative technology to enable proactive, quality monitoring of human safety of our products while continuously improving operational efficiency • Ensure PV systems are 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 ❯

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 … 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 More ❯