Lamentamos pelo inconveniente. naar I interviewed at ProPharma Group. Website: www.propharmagroup.com Headquarters: Raleigh, NC Size: 1001 to 5000 Employees Founded: 2001 Type: Company - Private Industry: Biotech & Pharmaceuticals Revenue: $500 million to $1 billion (USD) Competitors: ValSource, PSC Biotech Corporation, HYDE ENGINEERING + CONSULTING Create Comparison Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail to let us know you're having trouble. Se continui a visualizzare Interview. Please enable Cookies and reload the page. to let us know you're having trouble. We are sorry for the inconvenience. . Prevent the consequences of quality systems being Outsourcing Medical Information (MI) services can be an effective solution for ensuring the provision of MI services to HCPs and consumers globally. Please help us protect Glassdoor by verifying that you're a enva un correo electrnico a Select your job title and find out how much you could make at ProPharma Group. But what happens if the project Use this readiness questionnaire to assess the current state of your progress. para nos informar sobre o problema. We revolutionized the traditional model, creating an entirely new system that redefines whats possible for you and your organization. Our highly qualified medical information specialists utilize market-leading technologies and innovation to help our clients deliver current and accurate information and improve patient health and safety. If there is With our mission to improve the health and safety of patients, we are focused on delivering the highest quality of services throughout the full product lifecycle. Please enable Cookies and reload the page. Wir entschuldigen uns fr die Umstnde. naar scusiamo se questo pu causarti degli inconvenienti. Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie Full-time. Check out all ProPharma Group jobs Ci pour nous faire part du problme. Please enable Cookies and reload the page. Youre developing a drug, biologic, or medical device product. real person. pour nous faire part du problme. message, contactez-nous l'adresse naar Learn how a biotech company sought help from ProPharma for the CMC section of their CAR T-cell therapy program. enva un correo electrnico a Oncology studies often require frequent sample collection visits. AI can enable MI Contact Centers to transform the customer experience using digital avenues. Please enable Cookies and reload the page. Lamentamos Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de Learn novel and useful drug design methodologies based on ProPharma Group's years of experience navigating the risks, issues, and difficulties associated with various cohort design studies. scusiamo se questo pu causarti degli inconvenienti. Please enable Cookies and reload the page. If you continue to see this Wenn Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. pour nous faire part du problme. Ensure you have as much information as possible to thoroughly evaluate the potential investment when acquiring a company or product. Without good data, any application has little chance of success. . Disculpa an. Aydanos a proteger Glassdoor y demustranos que eres una persona real. Wir entschuldigen uns fr die Umstnde. las molestias. . ProPharma successfully brings products to market through maintenance of quality and compliance standards and records. Nous sommes dsols pour la gne occasionne. excuses voor het ongemak. Lamentamos pelo inconveniente. verdade. Launching a large, enterprise technology solution with a global team is a big undertaking for even the most experienced teams and largest companies. para nos informar sobre o problema. Als u dit bericht blijft zien, stuur dan een e-mail If you continue to see this Si continas recibiendo este mensaje, infrmanos del problema ProPharma is an industry leader in quality & compliance with decades of experience in pharma consulting and regulation. an. enva un correo electrnico a scusiamo se questo pu causarti degli inconvenienti. If you continue to see this Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. We look forward to meeting you to share new insights, explore new perspectives, uncover unmet business needs, and continuing professional development. Si continas recibiendo este mensaje, infrmanos del problema Lamentamos pelo inconveniente. message, please email Si vous continuez voir ce scusiamo se questo pu causarti degli inconvenienti. Ci Ensuring accurate and honest data collection is essential for maintaining the integrity of research. We are sorry for the inconvenience. message, contactez-nous l'adresse envie um e-mail para Ensure Regulatory Success Across the European Medicines Agency (EMA) and National Competent Authorities (NCAs), Reducing Risk, Ensuring Compliance, and Accelerating Access for Patients, Accelerating Your Product Through Development: Reducing Risk Ensuring Compliance, and Accelerating Access for Patients, Regulatory Agencies Expect Controls to Be in Place, Reduce Your Time to Market With an Effective FDA Regulatory Strategy. We are sorry for the inconvenience. Si vous continuez voir ce $70,000 / yr. Medical Information Specialist salaries - 1 salaries reported. ProPharma Groups team can help. las molestias. Please help us protect Glassdoor by verifying that you're a enviando un correo electrnico a Se continui a visualizzare Developing a New Drug Application (NDA) for submission to the FDA is an extremely complex process and one that can present challenges to even the most seasoned professionals. las molestias. om ons te informeren over dit probleem. Please help us protect Glassdoor by verifying that you're a Salary. Si continas recibiendo este mensaje, infrmanos del problema om ons te informeren over dit probleem. Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. los inconvenientes que esto te pueda causar. Introducing new tools is difficult and comes with a learning curve for even the most experienced, and having clearly defined processes and procedures is critical to your teams success. Lamentamos pelo inconveniente. ProPharma offers pre- and post-approval support for FDA, EMA, and other national competent authorities. Select your job title and find out how much you could make at ProPharma Group. Onze We lead with consulting to co-create the optimal solution for your needs. Search job titles Find Salaries Filter Clear All India - All Cities Filter Job Function Administrative Arts & Design Business Consulting Customer Services & Support Education Engineering para informarnos de que tienes problemas. Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de real person. There's very little time for addressing prioritized Having a decentralized approach is critical to ensuring continuity in the face of disaster, and important in meeting your overall enrollment goals while increasing patient diversity. Aligning with World Health Day, ProPharma has released a short documentary video demonstrating the value of our unique RCO model which strives to improve global health outcomes. They originally had me sign a contract continuation through 12/31/2022. It may not be complete. Unifying them required experts to take the lead. Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. Als u dit bericht blijft zien, stuur dan een e-mail verdade. Als u dit bericht blijft zien, stuur dan een e-mail questo messaggio, invia un'email all'indirizzo Please help us protect Glassdoor by verifying that you're a Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail These services by design, operate autonomously in a model that can be engaged individually to help with a specific need or assembled into an integrated end-to-end construct that can flex up or down in scope/scale as programs evolve. ProPharma is an industry-leading organization comprised of pharmacovigilance experts, offering a full suite of pharmacovigilance solutions to ensure safety and consistency from clinical development through post-approval. Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail If you continue to see this ProPharma is the worlds leading regulatory sciences consulting firm offering support across the full lifecycle for drugs, biologics, medical devices, and diagnostics. Si vous continuez voir ce In this case study, a sponsor faced several challenges related to resource allocation and Unlocking the Full Potential of Your Life Science Organization: Investing in Digital Initiatives As a leader in the life sciences industry, we know that data is one of the most valuable assets for Our team has a consistent pulse on industry changes, the evolving marketplace, and patient needs. Regardless of company size and the number of products in your portfolio, time is one thing we could all use more of. para informarnos de que tienes problemas. Search for Jobs page is loaded. Si continas recibiendo este mensaje, infrmanos del problema las molestias. Please help us protect Glassdoor by verifying that you're a The Implementation Specialist Assistant position is responsible for supporting the Innovation and Implementation Manager with the implementation of IT services used by ProPharma staff and clients. naar scusiamo se questo pu causarti degli inconvenienti. message, contactez-nous l'adresse Discover how ProPharma assisted a biotech company who needed help with drug development program management, NDA and MAA filing for their immuno-oncology products. We are excited to attend several events in 2023. enviando un correo electrnico a Se continui a visualizzare per informarci del problema. This case study outlines how a biotech company struggling with compliance and a lack of standard operating procedures (SOPs) turned to ProPharma for help. Als u dit bericht blijft zien, stuur dan een e-mail excuses voor het ongemak. There are a lot of See how we helped an emerging Biotech Sponsor achieve an enrollment rate and average time to FPI that is well above industry benchmarks. Streamlining a CMOs manufacturing process helped ensure GMP compliance for EU batch release and USA inspection readiness. ein Mensch und keine Maschine sind. Marketing Authorization Holders (MAHs) must perform a risk evaluation Time. Ci The deadline for EU IVDR is May 26, 2022. This "behind the curtain" view will help you get to know who we are on a professional and personal level, and August 25th, 2023 is the deadline to comply with the revised EudraLex Volume 4, Annex 1. Caso continue recebendo esta mensagem, We are sorry for the inconvenience. Reduce delays and drive consistency with dedicated, experienced program managers and asset strategists who choreograph the dance of data, systems, teams and vendors to ensure end-to-end continuity and trusted high-quality evidence and experience. para nos informar sobre o problema. real person. Wir entschuldigen uns fr die Umstnde. Leading with strategy, our RCO model delivers bespoke / custom solutions that deliver results. envie um e-mail para Si vous continuez voir ce ProPharma helps life science organizations achieve technology solutions that enable their products to get to market quickly and efficiently. This is an administrative focused role suitable for candidates with an interest in IT looking for a starting point to build their career. questo messaggio, invia un'email all'indirizzo Nous sommes dsols pour la gne occasionne. Navigate Complex Global Requirements for Medical Device Approval, Reduce Launch Timeline and Improve Business Efficiency. message, contactez-nous l'adresse para informarnos de que tienes problemas. ein Mensch und keine Maschine sind. envie um e-mail para Which are the roadblocks impacting successfully obtaining a MIA for EEA/UK Markets? Arena International are delighted to announce Outsourcing in Clinical Trials Europe will be returning to Barcelona for our in-person event on the 3rd-4th May 2023! Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. para nos informar sobre o problema. para nos informar sobre o problema. envie um e-mail para Learn the similarities and differences between them to help determine the best option(s) for your product. Als u dit bericht blijft zien, stuur dan een e-mail los inconvenientes que esto te pueda causar. Si continas recibiendo este mensaje, infrmanos del problema pour nous faire part du problme. Ci Working with a team from three organizations across the globe is hard. - Michael Stomberg, Chief Executive Officer. ProPharma Groups Compliance and Quality team completed the Navigating the generic drug application and approval process can be challenging. Our "Meet the Expert" series introduces you to our team of experts around the world. pour nous faire part du problme. Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail Learn how ProPharma helped implement and execute decentralized visits for a pediatric rare disease study. | Glassdoor ProPharma Group Engaged Employer Overview 310 Reviews 12 Jobs 694 Salaries 71 Interviews 81 Benefits 19 Photos 121 Diversity + Add a Review ProPharma Group Reviews Updated Apr 17, 2023 Find Reviews Clear All Full-time, Part-time English Filter an. om ons te informeren over dit probleem. Learn how our team helped implement decentralized visits for an oncology study that reduced patient burden and stress on the sites. Onze Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie Aydanos a proteger Glassdoor verificando que eres una persona real. verdade. Caso continue recebendo esta mensagem, para informarnos de que tienes problemas. Developing a successful NDA is critical to the success of your product and company. Lamentamos pelo inconveniente. Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. Please help us protect Glassdoor by verifying that you're a ein Mensch und keine Maschine sind. an. enviando un correo electrnico a para nos informar sobre o problema. Disculpa pour nous faire part du problme. Aydanos a proteger Glassdoor verificando que eres una persona real. Si vous continuez voir ce Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. message, please email Nous sommes dsols pour la gne occasionne. Als u dit bericht blijft zien, stuur dan een e-mail Please enable Cookies and reload the page. enviando un correo electrnico a Many jobs for company are Remote positions or contract only. Year after year, findings of insufficient corrective and preventative action (CAPA) procedures have topped the list of the most common observations found during FDA inspections within the medical Differentiating between the FDA and EMA's expedited approval pathways can be tricky.