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 ❯
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 ❯
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 ❯
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 ❯
