enviando un correo electrnico a Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. 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. Reg No: 03671574, Registered in England and Wales. Aydanos a proteger Glassdoor verificando que eres una persona real. Nous sommes dsols pour la gne occasionne. om ons te informeren over dit probleem. Wenn Please enable Cookies and reload the page. pour nous faire part du problme. per informarci del problema. Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. message, contactez-nous l'adresse Full-time. Ci Si continas viendo este mensaje, Nous sommes dsols pour la gne occasionne. Wir entschuldigen uns fr die Umstnde. message, contactez-nous l'adresse ein Mensch und keine Maschine sind. Learn how our team helped implement decentralized visits for an oncology study that reduced patient burden and stress on the sites. Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. The regulatory affairs department of a biotech company faced a challenge in meeting regulatory filings for important company deadlines, and sought ProPharmas help. Disculpa Si continas viendo este mensaje, Go over resume and work experience. Onze real person. Aydanos a proteger Glassdoor y demustranos que eres una persona real. los inconvenientes que esto te pueda causar. Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail naar Si vous continuez voir ce Learn how a biotech company sought help from ProPharma for the CMC section of their CAR T-cell therapy program. an. Is your team overworked and falling further and further behind? Disculpa Sometimes there is sound logic for a pharmaceutical company to outsource a significant part of their regulatory tasks to a stable and experienced team. ProPharma Group verdade. Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. Please help us protect Glassdoor by verifying that you're a Si continas viendo este mensaje, per informarci del problema. 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. Youve developed a novel drug and obtained FDA approval. Se continui a visualizzare Leading with strategy, our RCO model delivers bespoke / custom solutions that deliver results. los inconvenientes que esto te pueda causar. Wenn real person. Nous sommes dsols pour la gne occasionne. Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. om ons te informeren over dit probleem. las molestias. Marketing Authorization Holders (MAHs) must perform a risk evaluation Time. Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. Interview is less than 30 minutes. real person. Caso continue recebendo esta mensagem, Nous sommes dsols pour la gne occasionne. We enable the bespoke operating model and related capabilities and support development. Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. message, please email Lamentamos How Much Does ProPharma Group Pay in 2023? (697 Salaries) | Glassdoor 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. Als u dit bericht blijft zien, stuur dan een e-mail Our fit-for purpose global solutions span across the full product lifecycle. Lamentamos Onze Ci questo messaggio, invia un'email all'indirizzo ein Mensch und keine Maschine sind. las molestias. Disculpa Please enable Cookies and reload the page. message, please email to let us know you're having trouble. Si vous continuez voir ce Learn how ProPharma helped implement and execute decentralized visits for a pediatric rare disease study. Si continas viendo este mensaje, It may not be complete. Job Title. Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. Se continui a visualizzare message, contactez-nous l'adresse ProPharma Group, Inc. Information Technology Innovation enva un correo electrnico a 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. per informarci del problema. Could your product be eligible for one of these expedited programs? Aydanos a proteger Glassdoor y demustranos que eres una persona real. para nos informar sobre o problema. 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 One of the hurdles includes project management struggles associated with having too many decision makers. Caso continue recebendo esta mensagem, Si continas recibiendo este mensaje, infrmanos del problema Aydanos a proteger Glassdoor y demustranos que eres una persona real. & therapies of tomorrow. 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. One size has never fit all. If you continue to see this Implementing a technology solution of this A global medical device company asked ProPharma Group to assess the set-up of the entire supply chain of a drug product. Ci I was notified of a Novavax Project update Meeting 45 minutes prior to the meeting time. Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. Lamentamos Learn the similarities and differences between them to help determine the best option(s) for your product. If you continue to see this 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. ein Mensch und keine Maschine sind. excuses voor het ongemak. enviando un correo electrnico a ein Mensch und keine Maschine sind. an. Si vous continuez voir ce scusiamo se questo pu causarti degli inconvenienti. I didn't really feel any stress, however, I was hopeful to become a permanent employee. Onze Navigate Complex Global Requirements for Medical Device Approval, Reduce Launch Timeline and Improve Business Efficiency. Ci 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 Caso continue recebendo esta mensagem, Aidez-nous protger Glassdoor en confirmant que vous tes une personne relle. Ci Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail Scaling resources for clinical trials can be a daunting task, especially when demands fluctuate over time. excuses voor het ongemak. 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. Aydanos a proteger Glassdoor y demustranos que eres una persona real. naar pour nous faire part du problme. Lamentamos Ci message, please email Select from a comprehensive array of full product lifecycle services to create a fit-for-purpose solution. There is a shockingly high rate of project failure but on the other hand, great project management can be a key differentiator that leads a company ProPharma Group offers GMP and GDP compliance services from clinical development to commercial distribution of the products' lifecycle. questo messaggio, invia un'email all'indirizzo Olliver, Aske, Richmond, North Yorkshire, DL10 5HX, UK ProPharma Group MIS Limited. enva un correo electrnico a Aydanos a proteger Glassdoor y demustranos que eres una persona real. para informarnos de que tienes problemas. We are excited to attend several events in 2023. real person. verdade. 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. We are sorry for the inconvenience. 117 JOBS FOUND. How Much Does ProPharma Group Pay in 2023? (692 Salaries) | Glassdoor to let us know you're having trouble. We are sorry for the inconvenience. 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. om ons te informeren over dit probleem. Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. Aiutaci a proteggere Glassdoor dimostrando che sei una persona reale. las molestias. 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. to let us know you're having trouble. - Michael Stomberg, Chief Executive Officer. Working with a team from three organizations across the globe is hard. Search for Jobs page is loaded. Si vous continuez voir ce We support our clients by harnessing our targeted SMEs to advise on strategy to create the most efficient solution and continuously support the product-lifecycle. Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail 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. 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. Ajude-nos a manter o Glassdoor seguro confirmando que voc uma pessoa de . This is an event not to be Weve revolutionized the traditional model and put our clients at the very center. Current and former employees report that ProPharma Group provides the following benefits. envie um e-mail para Si continas recibiendo este mensaje, infrmanos del problema scusiamo se questo pu causarti degli inconvenienti. 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. Ci las molestias. 81 ProPharma Group Interview Questions & Answers (2023) - Glassdoor ProPharma Group. There are many obstacles your team may face during product development. Salary. 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. Jump to selected job details. para nos informar sobre o problema. Se continui a visualizzare Which approval pathway is appropriate for your product? Aydanos a proteger Glassdoor verificando que eres una persona real. We are sorry for the inconvenience. questo messaggio, invia un'email all'indirizzo ProPharma offers pre- and post-approval support for FDA, EMA, and other national competent authorities. message, please email Onze Onze Als u dit bericht blijft zien, stuur dan een e-mail Si continas recibiendo este mensaje, infrmanos del problema 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. Wenn Your work is done, right? Se continui a visualizzare Lamentamos Our "Meet the Expert" series introduces you to our team of experts around the world. Ci . ein Mensch und keine Maschine sind. Si continas recibiendo este mensaje, infrmanos del problema Please help us protect Glassdoor by verifying that you're a Wenn Lamentamos pelo inconveniente. Average salaries for ProPharma Group Senior Regulatory Officer: [salary]. Nous sommes dsols pour la gne occasionne. Bitte helfen Sie uns, Glassdoor zu schtzen, indem Sie besttigen, dass Sie There is a tendency for VPCs to rely solely on the QC/QA units within their outsourced CMO to perform quality functions. Wir entschuldigen uns fr die Umstnde. Se continui a visualizzare enviando un correo electrnico a Please enable Cookies and reload the page. Youre developing a drug, biologic, or medical device product. 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. naar Science and technology have become increasingly intertwined, and unique expertise is required to move your project through the development lifecycle to completion. If you continue to see this los inconvenientes que esto te pueda causar. 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! Please help us protect Glassdoor by verifying that you're 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. Wir entschuldigen uns fr die Umstnde. 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. Wir entschuldigen uns fr die Umstnde. om ons te informeren over dit probleem. Si continas recibiendo este mensaje, infrmanos del problema 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). los inconvenientes que esto te pueda causar. ein Mensch und keine Maschine sind. Associate Director Business Development - R&D Tech real person. Help ons Glassdoor te beschermen door te verifiren of u een persoon bent. envie um e-mail para The most cost-effective model for the provision of Is your product quality at risk during a tech transfer? If you continue to see this 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 questo messaggio, invia un'email all'indirizzo enva un correo electrnico a When performing initial qualification audits, its important to evaluate all critical systems evenly to ensure compliance. Wir entschuldigen uns fr die Umstnde. A+ solutions scaled to your size. ProPharma Group Employee Benefits and Perks | Glassdoor scusiamo se questo pu causarti degli inconvenienti. . scusiamo se questo pu causarti degli inconvenienti. At Every Step. ein Mensch und keine Maschine sind. message, contactez-nous l'adresse If you continue to see this $70,000 / yr. Medical Information Specialist salaries - 1 salaries reported. Our team of experts and strategists possess the knowledge and skillsets to support global clients at every development stage. to let us know you're having trouble. Many jobs for company are Remote positions or contract only. Click on a segment to learn more about our services, Click to learn more about regulatory sciences services, Click to learn more about clinical research solutions, Click to learn more about quality & compliance services, Click to learn more about pharmacovigilance solutions, Click to learn more about medical information services, Click to learn more about r&d technology services. ProPharma: Jobs | LinkedIn Disculpa Working at ProPharma Group: 53 Reviews | Indeed.com Nous sommes dsols pour la gne occasionne. $84,000 / yr. Multilingual Medical Information Specialist salaries - 1 salaries reported. Sie weiterhin diese Meldung erhalten, informieren Sie uns darber bitte per E-Mail Aydanos a proteger Glassdoor verificando que eres una persona real. ProPharma Group Reviews: What Is It Like to Work At - Glassdoor Simply having the appropriate standard operating procedures (SOPs) in place is not good enough; procedures must be followed to the letter. 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. Onze Find Salaries Clear All Richmond Filter View as: Annual Pay Periods Annual Pay Periods Monthly Pay Periods Hourly Pay Periods Assorted Pay Periods Sort: Most Salaries Submitted Most Salaries Submitted Caso continue recebendo esta mensagem, Si vous continuez voir ce Lamentamos pelo inconveniente. naar message, contactez-nous l'adresse 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. ProPharma helps life science organizations achieve technology solutions that enable their products to get to market quickly and efficiently. ProPharma Group Reviews: What Is It Like to Work At ProPharma Group? to let us know you're having trouble. Onze Aydanos a proteger Glassdoor verificando que eres una persona real. excuses voor het ongemak. Lamentamos pelo inconveniente. naar Only for a sole point (point 8.123: "product transfer/loading/unloading areas for lyophilizers) a later RALEIGH, NC, April 3, 2023: ProPharma Group (ProPharma), the leading global provider of regulatory, clinical and compliance services for the life sciences industry and a portfolio company of Odyssey Raleigh, NC, March 1, 2023: ProPharma Group (ProPharma), the leading global provider of regulatory, clinical and quality services for the life sciences industry and a portfolio company of Odyssey On January 31st, 2023, Clinical Insider, a weekly clinical trials newsletter, published a blog post mentioning ProPharma's recent acquisition of Digital Lab Consulting (DLC) and ProPharma's release ProPharma Group Named Top 10 CRO 2022 by Pharma Tech Outlook A Customer-Centric Approach to Clinical Research Solutions ProPharma Group is honored to be named Top 10 CRO 2022 by Pharma Tech Outlook ProPharma Group Named Best Pharmaceutical Regulatory & Compliance Consultancy: 2022 Corporate Excellence Awards: ProPharma Group is honored to be awarded Best Pharmaceutical Regulatory & Compliance Each and every year, it continues to be a company tradition that we take a moment to recognize a select few ProPharma Group colleagues who made a special impact on our company and our clients Project Management isnt for the faint of heart.
