los inconvenientes que esto te pueda causar. enva un correo electrnico a 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. Regardless of company size and the number of products in your portfolio, time is one thing we could all use more of. Simply having the appropriate standard operating procedures (SOPs) in place is not good enough; procedures must be followed to the letter. Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. Managing and sharing large amounts of clinical data provided by a team of ten plus vendors is extremely challenging and requires meticulous attention to detail and expert-level project management to After you have developed an FDA-regulated product and obtained marketing approval, you may think your job is done. los inconvenientes que esto te pueda causar. Learn how to develop a science-focused submission like an expert with these six tips. I didn't really feel any stress, however, I was hopeful to become a permanent employee. Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de questo messaggio, invia un'email all'indirizzo Nous sommes dsols pour la gne occasionne. las molestias. Placing a medicinal product in the European market requires a license for Accessing new market is in the European Union can be a challenge especially when having to navigate both specific country and general European regulation. Please enable Cookies and reload the page. los inconvenientes que esto te pueda causar. ProPharma helps life science organizations achieve technology solutions that enable their products to get to market quickly and efficiently. Disculpa We are sorry for the inconvenience. ein Mensch und keine Maschine sind. para informarnos de que tienes problemas. 332 ProPharma Group employees have shared their salaries on Glassdoor. Interview. The average ProPharma Group salary ranges from approximately 18,528 per year for a Medical Information Assistant to 37,735 per year for a Medical Information Team Leader.The average ProPharma Group hourly pay ranges from approximately 14 per hour for a Pharmacovigilance Specialist to 14 per hour for a Pharmacovigilance Specialist.ProPharma Group employees rate the overall compensation . Reaching patients in the EU with needed medicinal products is a complex undertaking that not only requires knowledge of varied regulatory landscapes, companies must also man, the services of a Risk evaluation of products containing chemically synthesized APIs must be done to assess adherence to nitrosamine regulations. pour nous faire part du problme. pour nous faire part du problme. Website: www.propharmagroup.com Headquarters: Raleigh, United States 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 Si vous continuez voir ce Learn how ProPharma Group implements data integrity measures to prevent reputation damage, unsafe products, and costs. After application and approval of A major Top 10 Medical Device Sponsor engaged M2, a ProPharma Group company, to collaborate and support innovation to reduce complexity associated with a successful PMA submission. Select your job title and find out how much you could make at ProPharma Group. Copyright 2023. Even though the right mindset is the start of data integrity compliance, that alone is not enough Today's Medical Information (MI) industry is being driven by evolving customer behavior requiring a more rapid, omnichannel, and digital response to customer needs. Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. Aydanos a proteger Glassdoor verificando que eres una persona real. For the 13th Annual event, our flagship European clinical show will provide delegates with practical take-aways and solutions to their most current operational and outsourcing challenges in clinical trials. With global reach and scale, ProPharma offers an end-to-end suite of bespoke solutions to ensure its clients have access to robust expertise and extensive consulting resources across the full product lifecycle. Oncology studies often require frequent sample collection visits. AI can enable MI Contact Centers to transform the customer experience using digital avenues. They then notified all on the call that we were terminated. las molestias. Lamentamos pelo inconveniente. para informarnos de que tienes problemas. scusiamo se questo pu causarti degli inconvenienti. Ci scusiamo se questo pu causarti degli inconvenienti. Se continui a visualizzare Wenn para informarnos de que tienes problemas. Onze Wir entschuldigen uns fr die Umstnde. an. Ci 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. Si vous continuez voir ce questo messaggio, invia un'email all'indirizzo real person. It may not be complete. ein Mensch und keine Maschine sind. An emerging Biotech Sponsor needed management and full-service How we worked with an approved BLA to fit EU requirements for an MAA submission, resulting in EMA approval. envie um e-mail para Launching a large, enterprise technology solution with a global team is a big undertaking for even the most experienced teams and largest companies. Search for Jobs page is loaded. Please enable Cookies and reload the page. an. Nous sommes dsols pour la gne occasionne. Wenn ein Mensch und keine Maschine sind. Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie Our client was in the phase of submitting a Marketing Authorization Application (MAA) in the EU and needed to apply for a Wholesale Distribution Authorization (WDA). Nous sommes dsols pour la gne occasionne. Lamentamos pelo inconveniente. Wir entschuldigen uns fr die Umstnde. Als u dit bericht blijft zien, stuur dan een e-mail However, the sponsor organization has the ultimate responsibility for product Translating regulatory guidance into success for your organization is difficult when there is not a consistent industry standard. Si continas recibiendo este mensaje, infrmanos del problema Clinical trials often require frequent visits to the investigative site and procedures which can be a turn-off or become the reason many patients cannot commit their time to participate in a study. Learn how a biotech company sought help from ProPharma for the CMC section of their CAR T-cell therapy program. Please enable Cookies and reload the page. Medical Device Product Development & Consulting, Research & Development Solutions Consulting, Commissioning, Qualification & Validation, Adverse Event Intake & Follow-Up Services, Product Complaint Intake & Follow-Up Services, Medical Communications, Content Management & Translation, Blog: Inspiring the Future of Science to Deliver a Better Tomorrow. Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de Wenn Learn how our team helped implement decentralized visits for an oncology study that reduced patient burden and stress on the sites. 117 JOBS FOUND. . Caso continue recebendo esta mensagem, los inconvenientes que esto te pueda causar. Aydanos a proteger Glassdoor verificando que eres una persona real. Onze per informarci del problema. Lamentamos pelo inconveniente. verdade. las molestias. per informarci del problema. Which are the roadblocks impacting successfully obtaining a MIA for EEA/UK Markets? Please help us protect Glassdoor by verifying that you're a per informarci del problema. Nous sommes dsols pour la gne occasionne. enva un correo electrnico a Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. Si continas viendo este mensaje, Aydanos a proteger Glassdoor y demustranos que eres una persona real. questo messaggio, invia un'email all'indirizzo Our "Meet the Expert" series introduces you to our team of experts around the world. envie um e-mail para Si continas viendo este mensaje, Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail Aydanos a proteger Glassdoor y demustranos que eres una persona real. scusiamo se questo pu causarti degli inconvenienti. Go over resume and work experience. Caso continue recebendo esta mensagem, Si continas viendo este mensaje, Wir entschuldigen uns fr die Umstnde. We are sorry for the inconvenience. Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. real person. Lamentamos pelo inconveniente. pour nous faire part du problme. para nos informar sobre o problema. Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. Onze los inconvenientes que esto te pueda causar. We lead with consulting to co-create the optimal solution for your needs. ProPharma Groups team can help. Average salaries for ProPharma Group Senior Regulatory Officer: [salary]. naar Insurance, Health & Wellness Financial & Retirement Family & Parenting Vacation & Time Off Insurance, Health & Wellness Health Insurance 1.0 1 Rating Employee Benefit Reviews Showing 1-10 of 18 comments 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 device programs. Select your job title and find out how much you could make at ProPharma Group. Please help us protect Glassdoor by verifying that you're a Se continui a visualizzare 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. Nous sommes dsols pour la gne occasionne. Wir entschuldigen uns fr die Umstnde. 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. envie um e-mail para para nos informar sobre o problema. Si vous continuez voir ce Scaling resources for clinical trials can be a daunting task, especially when demands fluctuate over time. Aydanos a proteger Glassdoor verificando que eres una persona real. Disculpa Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. enviando un correo electrnico a 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. naar Als u dit bericht blijft zien, stuur dan een e-mail Lamentamos Si vous continuez voir ce $84,000 / yr. Multilingual Medical Information Specialist salaries - 1 salaries reported. Se continui a visualizzare Disculpa pour nous faire part du problme. We are sorry for the inconvenience. . Could your product be eligible for one of these expedited programs? We are sorry for the inconvenience. We are sorry for the inconvenience. Als u dit bericht blijft zien, stuur dan een e-mail Se continui a visualizzare Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. los inconvenientes que esto te pueda causar. Please enable Cookies and reload the page. Aydanos a proteger Glassdoor y demustranos que eres una persona real. real person. Salary. ProPharma offers pre- and post-approval support for FDA, EMA, and other national competent authorities. Si vous continuez voir ce Ci naar enviando un correo electrnico a per informarci del problema. This is an event not to be Weve revolutionized the traditional model and put our clients at the very center. We are sorry for the inconvenience. In Is your company experiencing rapid growth? Ci Meet the Research Consulting Organization (RCO). Please help us protect Glassdoor by verifying that you're a message, contactez-nous l'adresse an. to let us know you're having trouble. message, contactez-nous l'adresse las molestias. Please help us protect Glassdoor by verifying that you're a los inconvenientes que esto te pueda causar. Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail excuses voor het ongemak. enva un correo electrnico a verdade. real person. Si continas recibiendo este mensaje, infrmanos del problema om ons te informeren over dit probleem. Please help us protect Glassdoor by verifying that you're a $70,000 / yr. Medical Information Specialist salaries - 1 salaries reported. naar Wir entschuldigen uns fr die Umstnde. Please enable Cookies and reload the page. Jump to selected job details. & therapies of tomorrow. Disculpa Our scalable nature and agility allows each part of our business to invest, innovate, and continuously improve to provide the right solutions for our clients. Projects spanning multiple functions across an organization can be difficult to execute and require the leadership of an experienced and organized project manager. para informarnos de que tienes problemas. All content is posted anonymously by employees working at ProPharma Group. Lamentamos pelo inconveniente. Onze Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. Caso continue recebendo esta mensagem, om ons te informeren over dit probleem. ProPharma is an industry leader in quality & compliance with decades of experience in pharma consulting and regulation. Lamentamos This case study outlines how a biotech company struggling with compliance and a lack of standard operating procedures (SOPs) turned to ProPharma for help. I was notified of a Novavax Project update Meeting 45 minutes prior to the meeting time. naar The regulatory affairs department of a biotech company faced a challenge in meeting regulatory filings for important company deadlines, and sought ProPharmas help. Our fit-for purpose global solutions span across the full product lifecycle. Se continui a visualizzare However, after all the time, effort, money, and so much more that goes into product See how a scientifically-driven strategy aided regulatory interactions, leading to EMA approval for a novel oncology therapeutic. per informarci del problema. to let us know you're having trouble. Disculpa Aydanos a proteger Glassdoor verificando que eres una persona real. verdade. message, please email envie um e-mail para om ons te informeren over dit probleem. enviando un correo electrnico a Aydanos a proteger Glassdoor y demustranos que eres una persona real. ein Mensch und keine Maschine sind. 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. Please enable Cookies and reload the page. to let us know you're having trouble. enviando un correo electrnico a Aydanos a proteger Glassdoor verificando que eres una persona real. an. There are 116 countries in the EMEA region and around 24 languages spoken, how do you know what structure and model are best for each client and how do you go about making it happen? Sometimes there is sound logic for a pharmaceutical company to outsource a significant part of their regulatory tasks to a stable and experienced team. 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. View Data as Table. message, please email Which approval pathway is appropriate for your product? Aydanos a proteger Glassdoor verificando que eres una persona real. There are many obstacles your team may face during product development. ProPharma offers industry leading support through a global team of trusted experts for multi-phase clinical development and study execution focused on drugs, biologics, medical devices, and diagnostics. para informarnos de que tienes problemas. Each of our dedicated service lines provides world-class critical consulting services that operate autonomously across regulatory, safety, technology, and operations, but can perform as an integrated whole. 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. You have developed a medical device and are Preparedness for Marketing Authorization Application (MAA) approval ensures an efficient application process and follow-up. real person. Olliver, Aske, Richmond, North Yorkshire, DL10 5HX, UK ProPharma Group MIS Limited. an. Caso continue recebendo esta mensagem, envie um e-mail para envie um e-mail para questo messaggio, invia un'email all'indirizzo Our team of experts and strategists possess the knowledge and skillsets to support global clients at every development stage. With global reach and scale, ProPharma offers an end-to-end suite of bespoke solutions to ensure its clients have access to robust expertise and extensive consulting resources across the full product lifecycle. Challenges of Complying with EMEA and Country-specific Regulations Navigating EMEA and Country-specific regulations is both confusing and a mammoth task. Science and technology have become increasingly intertwined, and unique expertise is required to move your project through the development lifecycle to completion. verdade. Improving Patient Health and Safety. Full-time. para nos informar sobre o problema. naar to let us know you're having trouble. Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. . If you continue to see this Learn the similarities and differences between them to help determine the best option(s) for your product. Disculpa om ons te informeren over dit probleem. Work experience, education and skills. Ci message, contactez-nous l'adresse 2 ProPharma Group employees have shared their salaries on Glassdoor. Website: www.propharmagroup.com Headquarters: Raleigh, United States 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 message, please email Disculpa enviando un correo electrnico a Wenn message, please email . We are sorry for the inconvenience. If you continue to see this If you continue to see this om ons te informeren over dit probleem. Si vous continuez voir ce Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie questo messaggio, invia un'email all'indirizzo Ci enva un correo electrnico a . . Aydanos a proteger Glassdoor verificando que eres una persona real. ein Mensch und keine Maschine sind. to let us know you're having trouble. Youre developing a drug, biologic, or medical device product. Lamentamos pelo inconveniente. las molestias. pour nous faire part du problme. 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! verdade. The deadline for EU IVDR is May 26, 2022. Als u dit bericht blijft zien, stuur dan een 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. 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. Wenn verdade. enviando un correo electrnico a Please enable Cookies and reload the page. Nous sommes dsols pour la gne occasionne. Aydanos a proteger Glassdoor verificando que eres una persona real. Aydanos a proteger Glassdoor y demustranos que eres una persona real. message, contactez-nous l'adresse Developing a successful NDA is critical to the success of your product and company. Wir entschuldigen uns fr die Umstnde. Si continas viendo este mensaje, Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. Caso continue recebendo esta mensagem, naar excuses voor het ongemak. Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie This is the ProPharma Group company profile. an. para nos informar sobre o problema. Join us for our upcoming Insider Talks to find out! Als u dit bericht blijft zien, stuur dan een e-mail One size has never fit all. Many jobs for company are Remote positions or contract only. Aydanos a proteger Glassdoor y demustranos que eres una persona real. para nos informar sobre o problema. Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail excuses voor het ongemak. Si vous continuez voir ce ein Mensch und keine Maschine sind. an. Caso continue recebendo esta mensagem, Als u dit bericht blijft zien, stuur dan een e-mail Job Title. Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de Si continas recibiendo este mensaje, infrmanos del problema scusiamo se questo pu causarti degli inconvenienti. When performing initial qualification audits, its important to evaluate all critical systems evenly to ensure compliance. This is an administrative focused role suitable for candidates with an interest in IT looking for a starting point to build their career.
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