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 and Clinical Trials solutions to clients in the life sciences … manage the most demanding processes 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 500,000 users worldwide , helping them to More ❯
in-class technology and scientific 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: Consulting Technology Programme Manager (PV … budget, and to high quality standards. They must be highly experienced, strategic thinker with deep domain expertise in software delivery for the pharmaceutical industry—particularly in the areas of pharmacovigilance, safety, and regulatory technology. Key Responsibilities: Define, lead, and manage the successful execution of complex, multi-workstream programmes for pharmaceutical clients. Align programme objectives with business strategy and ensure that … continuous improvement and contribute to the development of enterprise-level project and programme delivery methodologies, frameworks, and governance structures. Ensure all programme activities are compliant with industry regulations, including pharmacovigilance standards (e.g., GVP, FDA, EMA) and data privacy laws (e.g., GDPR). Essential Experience and Qualifications: Bachelor's or Master's degree in Computer Science, Information Technology, Project Management, or More ❯
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 ❯
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 ❯
/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 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 the UK. Compensation based on … manage the most demanding processes 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 500,000 users worldwide , helping them to More ❯
Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan. Everest also recently completed the acquisition of August Research. August Research is a European CRO that provides Clinical Operations and Pharmacovigilance services to a wide variety of pharmaceutical and biotechnology clients. The Company has worked on over 120 projects for Phase I-IV clinical trials across multiple therapeutic areas including cardiovascular More ❯
new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle.With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and 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 ❯
