Nordstrom Supplier Diversity Program, Extraordinary Humans Muscles Transcript, Articles O

TICKETED. March 14 . The company specializes in end-to-end services supporting drug discovery, precision medicine and clinical development for smarter clinical studies. CROMSOURCE operates offices across Europe and North America. www.precisionformedicine.com. Attendees. News and Events - Ergomed PLC Complimentary. GlobalPlus Diagnostics on LinkedIn: Outsourcing in Clinical Trials At UCSF he co-invented suitable PEGylated lipids to make the very first PEGylated liposomes. Greenphire is the industry leader of clinical payment technology, designed to improve the way research professionals work. Dr. Raymond completed her doctoral training in molecular biology at University of California San Diego and post-doctoral training in molecular biology at Memorial Sloan-Kettering in New York City, New York, USA. Find out about the events you can meet the Caidya team at and stay updated about the latest conferences and clinical research events. The therapeutic areas include: Cancer, CV, CNS and infectious diseases. Can you share some of your workflow procedures? www.maxisit.com/ctos/. This conference will explore the latest regulatory updates, global clinical trials, advanced technologies and more. Agilex Biolabs operate a fully quality-assured, FDA-inspected laboratory (ISO/IEC17025 and OECD GLP). Kardia is the first AI-enabled platform to aid patients and clinicians in the efficient detection of atrial fibrillation, the most common arrhythmia and one associated with a highly-elevated risk of stroke. Conduct of clinical trials are increasingly becoming expensive. Clinical Trials Conferences | Meetings 2023 | World BI Headquartered in Uppsala, Sweden, Viedoc also has offi ces in America, France, Japan, Vietnam, and China. Our experienced project managers and global network of linguists are supported by proven processes and cutting-edge technology. AWT Healthcare manufacturers clinical trial labels. vial.com. European Union Clinical Trial Regulation: Strategic Considerations, Hyatt Regency San Francisco Airport Hotel The main program of the conference is discussion and debate on the outsourcing of clinical research. http://www.datacubed.com/. Drug development Conferences | Meetings | Events | Symposiums Frontageis a CRO providing integrated, scientifically-driven research, analytical and product development services throughout the drug discovery and development process to enable biopharmaceutical companies to achieve their drug development goals. Estela is an exceptional community engagement liaison for both English and Spanish speakers. Dr. Parapiteva is an experienced regulatory professional with over 24 years in the pharmaceutical industry/clinical research organizations. Jay is responsible for managing the creation and design of product features and new capabilities for Trial Interactive. www.careaccess.com. Emmes acquired Casimir in March 2022, and the . March 1 - March 2,2023 Outsourcing in Clinical Trials West Coast. www.eclinicalsol.com. AliveCor protects its customers with stringent data security and compliance practices, achieving ISO 27001 Certification, SOC 2 Type 2 Certification and HIPAA compliance attestation. Outsourcing in Clinical Trials Europe 2023. http://www.mlm-labs.com. http://www.medable.com/, To learn more , please visit our website - In her role at Nevro, Frances is responsible for leading the data management team, driving the adoption of new technologies and innovative data management processes to bring new treatments to patients. Over the years, Lin has achieved success at both large corporations and startups. To learn more , please visit our website - eClinical & Clinical Data Management Innovation Conference 2022 . Previously she served as Head of Clinical Outsourcing and Analytics for BioMarin Pharmaceuticals, where she was responsible for vendor contractual, relationship and financial management. Promedica International is a privately held, full-service CRO providing clinical trial services for the medical device, biotechnology and pharmaceutical industries. YPrimescloud-based technology streamlines clinical trial data collection and management. 200+. This conference will focus on topics such as bioethics, regulations, patient recruitment, site selection, data integration & strategy, and many more. Held annually in Paris and online, this event unites 5,000 attendees and 360 exhibitors centered around innovation, networking, and education. ), pharmacovigilance and safety solutions, translation and language services, and call center support. . assisTek has been paving the way for integrating technology and data collection in clinical trials for over 25 years. Ndidi also leads the X2 Women in Biotech Group speaker series and is one of the founding members of the UltraMosaic Employee Resource Group. Dr. Jankicevic is a sought-after speaker, and author of numerous articles in peer-reviewed and trade journals. Clinical Trials 2023. Clinical Services. Swiss Biotech Day 24th April 2023 to 25th April 2023 Basel, Switzerland. He has supervised the management of a clinical portal, eTMF, CTMS, RTSM, EDC, Coding and Grants solutions. The Budget Conundrum. Our digital solutions enable sites to be more productive, with online study training, study eBinders (eISF), digital study alerts and SUSARs, patient visit guides, and a wide range of study tools, available via web portals and mobile apps. Arena International are delighted to announceOutsourcing in Clinical Trials West Coastwill be returning to Burlingame for the annual event onMarch 1st& 2nd2023! Henry earned his B.S. Celerion provides full study services including statistics, data management and biostatistics (including PK/PD analysis), and bioanalytical services. www.curebase.com, To learn more , please visit our website - To learn more , please visit our website - Clinical Research Conferences in 2023/2024/2025 - World Academy of May 02-03, 2016 Chicago, USA. THREAD is a leading provider of a proprietary, decentralized research platform and suite of supporting services used by biopharma, CROs and life science organizations to remotely capture data from participants and sites during, in-between and in lieu of in-clinic visits. His most recent activity is as CEO and Founder of QuiVivePharma, a company he took from inception to a FDA face-to-face PreIND meeting in just 1 year. She is driven by listening and incorporating the patient voice and by finding innovative ways to improve the patient experience. Meghan serves as the VP, Clinical Trial Financial Management at Medidata driving roadmap and strategy across our Grants Manager and Site Payments products. degree in Neurobiology and is the author of several peer-reviewed papers in prostate cancer and premature ovarian failure. Read more. I look forward to being in the Bay Area in early Lee King on LinkedIn: #octwestcoast2023 #clinicalresearch #lifesciences #outsourcing In his role as BD lead, he is responsible for many aspects of the companys planning and operations. Mr. Chu was also the Import Program Manager (IPM) for the FDA Los Angeles District. Our high-caliber project management, clinical monitoring, medical safety, data management, biostatistics, regulatory affairs and quality assurance capabilities make us a valued partner. The Global Clinical Trials Connect 2022 will focus on futuristic advancements in the clinical research industry and clinical trials. Altasciences helping sponsors get better drugs to the people who need them, faster. Arena International are delighted to announce that our Outsourcing Clinical Trials Europe event is returning to an in-person format in 2022. 2023 edition of Outsourcing in Clinical Trials East Coast will be held at King of Prussia starting on 23rd May. Outsourcing in Clinical Trials (OCT): Medical Devices Europe 2022 We provide a comprehensive digital solution for Ph 1-4 studies with enterprise-level capability that is configurable to be fit for purpose to support biopharmaceutical companies, CROs and research sites. Dr. David Anderson is a Senior Scientist at Clinical Ink, where he focuses on the development of digital biomarkers in decentralized and remotely-monitored clinical research. Our Sponsor Edition includes dedicated applications for clinical study planning and budgeting, outsourcing and forecasting. Explore and learn more about Conference Series : World's leading Event Organizer. To learn more , please visit our website - Clinical Trials Innovation Programme 2023 is the only platform to . Oversight with less presence how to make this work, Effectively building strong working relationships remotely, Strategies to deliver training and upskill your team, Handling hard discussions with your CRO/partner when you cant meet in person, Optimizing communication channels/effectiveness with your CRO partner and team, Maintaining a positive working relationship prioritizing and building strategies from the outset, Clinical trial timelines are lengthy and on average a Phase 3 trial can take between 1-4 years. These conferences closely focus on the advancements in clinical research and trials. Mural Health is a participant management platform that helps manage & streamline the trial experience for patients and caregivers. KPS is a global, innovative, Clinical Outsourcing Provider delivering clinical trial monitoring, management and quality oversight services to pharmaceutical, biotechnology, medical device, and related industries. Founded in 1976, ACRP is a Washington, DC-based non-profit organization with more than 13,000 members who work in clinical research in more than 70 countries. Pro-ficiency converts training from a cost center to a powerful quality improvement system. Agilex Biolabs is the leading Australian Bioanalytical CRO providing regulated Bioanalysis to support clinical trials. Altasciencesis a forward-thinking, mid-size contract research organization offering pharmaceutical and biotechnology companies of all sizes a proven, flexible approach to preclinical and early phase clinical studies, from lead candidate selection to proof of concept. Our simulation-based protocol training prevents study errors, guarantees timely SIV, and frees up thousands of hours for your study team and site-staff. CA; X-Mine, CA; Delphian Pharma, CA and Certum LLC, CA). Bruce started his career on the faculty in the Chemistry Department at Purdue University where his independent research focused on neuronal signal transduction. Helping you take advantage of the speed of study start-up and R&D tax incentives in Australia and allow for smooth trial transition in the US. https://www.trilogywriting.com/. She has extensive experience in building quality organizations, overseeing Phase 3 global clinical trials, supporting marketing authorization applications in the US and EU, and managing pre-approval inspections leading to multiple product approvals and launches. Dr. Cunningham has over 15 years experience in clinical leadership position in medical device industry, overseeing a full spectrum of clinical development programs ranging from FIM to pivotal to post-market phases. AliveCor is a privately-held company headquartered in Mountain View, Calif. Consumer or Personal ECGs are ECG devices available for direct sale to consumers. To learn more , please visit our website - https://www.calyx.ai. Panellists will discuss the challenges and tech barriers with DCT. With offices in over 100 cities worldwide, TransPerfect is the ideal partner to ensure that your global launch makes a global impact by driving quality, mitigating compliance risk, and enhancing patient engagement. Our customized and scalable solutions improve the quality and execution of clinical trials while mitigating costs and allowing clients to retain strategic control. Subsequently completed a Neurology Residency at Columbia University with additional Fellowship training in Neuro-Oncology at the Mass General Brigham program. NikZ shows promise against other important fungal diseases. Long term solutions: could reducing the site certification process be a realistic solution? Wendi is currently the Executive Director, Global Medical Affairs Evidence Generation COE at BioMarin Inc. where she oversees global operational strategy and execution for programs in the post-approval setting. Discover effective strategies for outsourcing clinical trial operations to ensure trials run smoothly and within budget . DGE invites you to return to the industry's first, most detailed, and most trusted conference on this topic - our 7th Decentralized & Hybrid Clinical Trials Summit. Pharmaceutical Development. His clinical trial experience spans from set-up to delivery across all phases in a wide variety of disease and therapeutic areas. La Jolla, CA. For the past 10 years, Estela has co-facilitated support groups, led, and participated in educational symposiums, advocated locally and nationally. http://www.novotech-cro.com/, To learn more , please visit our website - Clinical Trial Conferences to attend in 2022 - McDougall Scientific THREADs platform and supporting services are helping customers to shorten study launch timelines, reduce study budgets with Virtual Visits, and bring studies from the clinic to patients homes. Debashish earned a PhD in Computer Science from the State University of New York at Buffalo, specializing in the application of AI techniques in document analysis. Employee turnover continues to impact global market for talent. ARENSIAs speed and data quality provide our Partners/Sponsors with a strategic advantage across the entire lifecycle of a project, as they can progress their novel compounds much faster to later phases of research. She was an assistant professor at Loyola University Chicago and a practicing vascular surgeon in Shanghai, China. Datacubed applies innovative solutions for the capture of active and passive data for engagement with patients in in-person, hybrid, or fully virtual clinical studies. www.myonex.com. Our goal each day, every day is to make sure our partners have whatever they need when and where they need it to execute a successful clinical trial, while also minimizing delays, unnecessary costs, and surprises. Medocitys platform is the only solution that provides a fully interactive clinical trial ecosystem enabling early decision making and safety monitoring in real time. Exploring new science and a futuristic perspective on AB/AM drug development, Exciting growth of artificial intelligence in medicine, A framework on development of artificial intelligence in medicine, The power of public attention and funding, Business opportunity of artificial intelligence in medicine, What they like to see in an outsourced partner organization, What they would like a partner to know about them / how they work. I went into industry for post-doctoral studies at the biotechnology research center at Ciba-Geigy Corp. (Novartis) and have over three decades of academic and industrial research and senior management experience in protein and metabolic engineering, bio-based manufacturing, and drug discovery / development. To learn more , please visit our website - Frances has an undergraduate degree in Physiology and a PhD in medical science from the University of Sydney. Data-driven operations and oversight with elluminate. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionalscollaborateswith biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Dr. Cunningham came from academic background. www.medocity.com, To learn more , please visit our website - To learn more , please visit our website - To collaborate with CISCRP for your upcoming event, please contact Joan Chambers at jchambers@ciscrp.org or Lindsey Elliott at lelliott . Our Australian phase I facilities are in Melbourne and Brisbane, and our US phase I facility is located in Minneapolis. www.zigzagassociates.com. RT1 Conducting a study when there is minimal education, Hang Nguyen, Sr. Director, Clinical Affairs, Materna Medical, RT2 Navigating the complex spiderweb of multiple vendor relationships, Sarah Mullen, Vice President of Clinical, HeartFlow, RT3 Training Strategies for a Novel Therapeutic Medical Device, Ann Louise Armstrong, Senior Manager of Clinical Affairs and Field Operations, Ancora Heart, - How the process started and steps taken, - Assessment of eligibility and submission, - Lessons learnt - how it helped and what we did, what we companies can learn and do better, Discussion focusing on Real World Data; an overview of opportunities and challenges in working with RWD/RWE, Ted Chun, Director, Global Clinical Shared Services, Stryker Neurovascular, RT2- Navigating the complex spiderweb of multiple vendor relationships, RT3- Training Strategies for a Novel Therapeutic Medical Device, Ann Louise Armstrong, RN, MSN, CCRC, CCRA, Senior Manager of Clinical Affairs and Field Operations, Ancora Heart. Karl has collaborated with the world's top 20 pharmaceutical companies and has extensive experience in patient-centered outcomes research, eCOA strategy, and drug development. . Specializing in clinical development and staffing solutions, we offer a flexible approach to ensure our clients unique needs are supported. She has authored or co-authored 10 publications and has been an advocate for STEM education throughout her career. Acceleration of clinical development in the worlds fastest growing region, Biotech Market Performance and the impact on Clinical Trials and Operations. He received M.Sc. Arena International are delighted to announce the Outsourcing in Clinical Trials Southern California Event will be returning to California's La Jolla on September 26th & 27th 2023! Prioritizing patient diversity. Bruce earned his doctorate in biochemistry from UCLA and completed a postdoctoral fellowship at the University of California Berkeley. Executive Director, Clinical Outsourcing and Alliance Management, BridgeBio Pharma, Inc. VP Digital Transformation Strategy, Medable, Sr. Director, Clinical Operations NGM Bio, Vice President, Drug Development, Alto Neuroscience, VP Clinical Trial Financial Management, Medidata, Product Director, Decentralised Trial Technology at YPrime, Health Technology - Clinical Research, Meta, Director, eCOA Science & Consulting, Clario, Associate Director, Quality Culture Excellence, Ultragenyx Pharmaceutical, Solutions Consultant, eClinical Solutions, Associate Director of Clinical Operations, CymaBay Therapeutics, Associate Director, Global Regulatory Clinical Services, Global Outsourcing Director, Development Operations, Ascendis Pharma, Sr. Clinical Operations Professional, Imago BioSciences, Senior Director Of Clinical Affairs , Materna Medical, RN, MSN, CCRC, CCRA, Senior Manager of Clinical Affairs and Field Operations Ancora Heart, Deputy Program Director, Office of Medical Devices and Radiological Health Operations (OMDRHO), ORA, FDA, Director, Global Clinical Shared Services at Stryker Neurovascular, Vice President Of Clinical Affairs, Endogenex, Director, Clinical Programs, Clinical Affairs, ReCor Medical, Director, Database Management, Nevro Corporation, Director Global Patient Safety- Device And Digital Health, AstraZeneca, Medical Director, Patient Safety Physician Digital & Devices, AstraZeneca, VP Quality Assurance, Regulatory Affairs And Clinical, IceCure Medical, Vice President, Product Management, Anju Software. Improving the patient experience through user-focused design. Formed through the merger of IMS Health and Quintiles, IQVIA has more than 58,000 employees worldwide. Previous roles within both CRO and Sponsor organizations which provide valuable perspective from both sides of the industry. The two day, in person conference, Outsourcing in Clinical Trials will deliver top-quality content from industry experts covering all aspects of operational . What can we do to take advantage of high prevalence of disease in populous countries but systems are either rudimentary or non-existent? www.tranquilclinicalresearch.com. Vice President, Clinical Operations, Corvus Pharmaceuticals Inc. Assistant Commissioner for Import Operations, U.S. Food and Drug Administration, Director, Global Patient Engagement and Advocacy, Acceleron Pharma, Associate Director, Site Contracts & Budgets Deciphera Pharmaceuticals, LLC, Program Director, Office Of Medical Device And Radiological Health Operations, FDA. Were a global provider of comprehensive drug development solutions, including consulting, clinical operations, biometrics, and clinical pharmacology across a variety of therapeutic areas. Dr Jankicevic holds Doctor of Medicine degree, Master of Medical Sciences degree, and Board-certification in Dermatology and Venereology from the University of Belgrade, Serbia. Their services include clinical monitoring, clinical monitoring oversight, clinical trial management, data management, biometrics, and medical writing. GreenLight Clinical is a physician-led, boutique full-service clinical CRO with its own central clinical, bioanalytical, histopathology laboratories in Sydney, Australia. Funwie strives to do meaningful work that combines and applies her bioethics background while prioritizing and addressing health equity in the context of clinical studies, patient experience, and policy. http://catalystcr.com/. . Allucent is on a mission to help bring new therapies to light by solving the distinct challenges of small and mid-sized biotech companies. She is currently the Founder and CEO of Strategikon Pharma, developer ofClinical MaestroTM, the industrys only end-to-end cloud-based platform for clinical trial budgeting, sourcing and budget management including strategic alliance/partnership management. . Join Premier Research at Outsourcing in Clinical Trials Southern California 2022 as it returns for its 9 th annual event. How applying behavioral science insights can better inform the way we do patient engagement. ICACB 2023: Applied Clinical Biostatistics Conference, Rio de Janeiro (Feb 16-17, 2023) ICAHIPHIM 2023: Advanced Healthcare Informatics and Public Health Informatics Management Conference, New York (Feb 16-17, 2023) ICCPP 2023: Clinical Psychiatry and Psychology Conference, Barcelona (Feb 16-17, 2023) ICEPNR 2023: Exercises for Pediatric . He has extensive experience helping sponsor companies make their trials a reality across a range of projects from first in human to phase iv. Q2 Solutions is a leading global clinical trials laboratory services organization that helps biopharmaceutical, medical device and diagnostics customers improve human health through innovation that transforms science and data into actionable medical insights. Axiom Exhibiting at Outsourcing in Clinical Trials New England 2022 Our comprehensive solutions include clinical trial management technology and services (TMF services, eTMF, CTMS, regulated content management, etc. Pro-ficiency ensures that everyone in your study is compliant with all training requirements. It is the go-to solution in over 1,000 sites and 40 countries enabling investigators and sponsors to simply record, review, anonymise and submit assessments to regulatory bodies. We have expanded our product line to include Medical Device Labeling through AWT Labels & Packaging. OUTSOURCING IN CLINICAL TRIALS EUROPE 2022 - HealthManagement.org Includes management of the RFP process for outsourced services as well as contract/proposal and budget negotiations, vendor selection, and vendor oversight/relationship management. Whether you require ad hoc support or a team to partner with on audit programs, we have the people, the expertise and the experience to provide the assistance you need. Ms. Lea is the Director of Global Patient Engagement and Advocacy for Acceleron, a wholly-owned Subsidiary of Merck. Before joining Clinical Ink in 2021, he was an Assistant Professor in the Department of Ophthalmology & Visual Sciences at the University of Nebraska Medical Center. Does it offer a solution? Caroline is experienced in the planning and execution of global clinical drug trials in the European, North American, Latin American, and Asia Pacific regions. To learn more , please visit our website - To learn more , please visit our website - ACM provides a powerful combination of operational excellence, scientific expertise and unsurpassed global service to customers in more than 65 countries. Based outside Philadelphia, Pennsylvania, we pride ourselves on being boutique by design and always customer focused. http://www.premier-research.com/, To learn more , please visit our website - www.deeplink-medical.com. Henry is a Vice President of Data Sciences at Medidata. She has over 22 years of experience overseeing GxP quality and compliance for all phases of drug development for biologics and small molecules. She has extensive experience in leading data management activities for multiregional clinical trials in all phases and several therapeutic areas. Dr Morimoto has over 25 years of industry experience in leading project teams in the development of innovative medicines, providing guidance in the design and execution of preclinical, clinical and regulatory strategies with a therapeutic focus in Parkinsons, Alzheimers and frontotemporal dementias. We are focused on helping our clients to address their most significant and complex drug discovery and development challenges. Our experts are ready to discuss how our solutions can best support your live studies. To learn more , please visit our website - Wed, 25 May 2022, 18:00 WebSite. Brandi Coffin has been in the medical device industry for over 15 years with various roles in post market surveillance, quality, compliance and patient safety. Liza has extensive experience in managing and overseeing phase I-IV clinical trials globally as well as building and growing clinical operations teams in oncology, cardiovascular, metabolic and liver diseases, HIV and trials in gene therapy. AbbVie reports rise in full-year 2022 net revenues; Teva Pharmaceutical reports 5% fall in Q4 2022 revenue; Merck reports 2% increase in worldwide sales in Q4 2022; Companies.