Includes management of the RFP process for outsourced services as well as contract/proposal and budget negotiations, vendor selection, and vendor oversight/relationship management. November 28-30, 2016 San Antonio, USA. Alton Sartor completed a combined MD/MBA from Tulane University. Alexis Garelli has over 15 years of diverse healthcare information and pharmaceutical software technology experience. www.flexdatabases.com. Operating in 49 countries across the globe, KPS Life is committed to working together with its clients through a hands-on operating model rooted in a partnership approach. Medidata is leading the digital transformation of life science, with the worlds most used platform for clinical development, commercial, and real-world data. Wednesday, 28th Sep 2022 - Thursday, 29th Sep 2022 . Digital health technologies and biomarkers in clinical trials requires the highest standards of data collection, transmission, security, quality, and analysis. Triomics is a technology company offering an enterprise-grade platform for clinical trial sites to automate data collection practices. Combining patient-reported health data, personal medical records, and conversations in the Inspire community uncovers critical insights unattainable with traditional research methodologies. To keep up to date with latest news, follow Almac Group on Twitter and LinkedIn or visit almacgroup.com. http://www.pcmtrials.com/, To learn more , please visit our website - To learn more , please visit our website - ), both from Duke University where I was also an undergraduate. April 28-29, 2016 Dubai, UAE. 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. To learn more , please visit our website - Embassy Suites Raleigh-Durham Research Triangle, Cary, NC. At Trilogy, medical writing is our passion. https://lifesciences.transperfect.com/, To learn more , please visit our website - Cognizing & mitigating Does AI-ML offer a solution? She has worked at several companies in positions of increasing responsibility including VP of Quality at InterMune (acquired by Roche) and Director of Quality at CV Therapeutics (acquired by Gilead). We have expanded our product line to include Medical Device Labeling through AWT Labels & Packaging. Electronic clinical outcome assessments (eCOA)and interactive response technology (IRT) platforms introduce greater speed, precision and data quality to clinical trials. Panellists will address the advantages of DCT; from taking the trial to the patient to boosting recruitment. Currently a Medical Director/Patient Safety Physician Digital & Devices at Astrazeneca. She currently serves as Vice President of Clinical Affairs at Endogenex, a medical device company developing innovative solutions for the treatment of Type 2 diabetes. Emvenio Research is transforming how patients and care-givers engage in and experience clinical research, To learn more , please visit our website - A healthy discussion on different disciplines in pre . The company specializes in end-to-end services supporting drug discovery, precision medicine and clinical development for smarter clinical studies. SDC delivers top-tier clinical trial services to pharmaceutical, biologic and device/diagnostic companies. To learn more , please visit our website - http://www.heartcorsolutions.com. For over 25 years, Altasciences has been integrating into clients projects to help support educated, faster, and more complete early drug development decisions. I will be there with my colleague Georgi Govedarov, come visit us at booth Isidora Teodorovi on LinkedIn: I am very excited to be attending Clinical Outsourcing Group UK this year ACM Global Laboratories is one of the largest global independent central labs in the industry. www.greenlightclinical.com, To learn more , please visit our website - Our Ergomed team is looking forward to exhibiting at Outsourcing Clinical Trials - Texas 2022, December 7th & 8th . To learn more , please visit our website - With locations in the US and EU, Catalyst offers highly flexible and customized, customer-centric solutions from Global Resourcing and FSP, to Full Service Managed Solutions, with a focus on oncology product development. The therapeutic areas include: Cancer, CV, CNS and infectious diseases. We contribute to a safer and better world by helping our sponsor clients accelerate drug and device approvals to market. Advantages of working alongside grass root organisations and PAGs what groups are out there? Topics include feasibility & site selection, clinical data & technology, patient engagement & enrollment, risk-based monitoring, and budeting & clinical outsourcing. . Our deep therapeutic-area expertise, coupled with Direct Data Capture, eCOA, eConsent, telehealth, neurocognitive testing, and digital biomarkers advancements, drive the industry standard for data precision and usher in a new generation of clinical trials. Reem enjoys working in startups bringing forward long-term vision and strategies. In addition to several peer reviewed publications and patents he published two volumes on, Process Chemistry in the Pharmaceutical Industry and currently is working on the third volume entitled, Bioprocessing, Bioengineering and Process Chemistry in the Biopharmaceutical Industry jointly with the bio-process leaders at Pfizer. 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. Why the current state of trials makes it difficult for patients to participate in research, How and when to incorporate patient insights into your programs, How to create a business case to garner support for investing in solutions, The benefit for the study sponsor, and other stakeholders, for investing in solutions to make it easier to be a participant, Barriers to patient participation with a focus on the barrier that became the impetus of the model, Delving into benefits of Patient Navigators and challenges with consistent comprehensive support for patients, Exploring the Enhanced Patient Support Services, Cover proactive strategies to address performance risk and protocol deviations, How to apply performance data from simulation-based training to manage risk areas, Discuss how to interpret and apply learning results to optimize and de-risk your DCT, Rethinking your site management strategy to minimize overburdening sites, dependant on the phase of your study, Pinpointing how site turnover impacts the sponsor and how to help reduce it whilst keeping patient care front of mind. Each nurse is trained, tested, and certified as a Certified Mobile on an annual basis in the principles of clinical trial research, GCP, Nurse Guidelines and IATA. It is a 2 day event organised by Arena International Events Group and will conclude on 24-May-2023. Clinical research professional with 25 years of experience in clinical and medical affairs, most recently as Director of Clinical Affairs and Associate Director of Medical Affairs for a global medical device manufacturer focusing on endovascular and surgical repair of aortic disease. With more than30 years of experience in over 60 countries, our individualized partnership approach provides experience-driven insights and expertise to assist clients in successfully navigating the complexities of delivering novel treatments to patients. Our company is committed to improving all lives touched by clinical research and we address the hopes of patients and healthcare professionals with industry-leading services and technology in life sciences. Why expert partners and staff matter; what metrics dont tell. PCM TRIALSscreens, hires, trains and manages all of our own Certified Mobile Research Nurses who conduct clinical trial visits in the subjects homes. Since 2003, Conversis has supported our life sciences clients to successfully and effectively communicate with patients and medical professionals worldwide. Learn more atwww.clinone.com. http://www.clindatrix.com/. Explore and learn more about Conference Series : World's leading Event Organizer. His goal is to help you accelerate your clinical research career and be a more effective leader. The elluminate Clinical Data Cloud provides one source of truth for clinical and operational data to manage trials across sources. Examining how, even as a small company with limited resources you can successfully introduce time and cost saving QMS measures. The conference will bring together pharmaceutical and biotech experts to connect and explore solutions to current challenges associated with clinical trials. Combined, our clinics offer over 200 beds. Discover effective strategies for outsourcing clinical trial operations to ensure trials run smoothly and within budget . To learn more , please visit our website - To learn more , please visit our website - As a supervisor, he had the opportunity to manage an Import Field Operation Team, an FDA team in the Centralized Examination Stations (CES), and the Los Angeles International Mail Facility. www.precisionformedicine.com. CROMSOURCE operates offices across Europe and North America. Register. Were your solution. Meraf Eyassu is a Executive Director of Clinical Operations at Terns Pharmaceuticals. Mr. Chu was also the Import Program Manager (IPM) for the FDA Los Angeles District. Online event and networking. Developing and supporting your quality initiatives from Day 1, the Harbor team is committed to quality through each functional service we provide. Bruce started his career on the faculty in the Chemistry Department at Purdue University where his independent research focused on neuronal signal transduction. The impact DCT has on diversity, equality and inclusion (DEI) have we finally managed to tap into under-represented communities? Mr. Luciano joined Corvus Pharmaceuticals in 2018 and has served as Vice President of Clinical Operations since 2021. Parexel Recognized by Frost & Sullivan with 2022 Global Customer Value Leadership Award . https://www.propharmagroup.com/. Sun, 24 Apr 2022, 09:00 End. www.viedoc.com, To learn more , please visit our website - Proven track record of coordinating teams in order to meet tight deadlines, set and communicate expectations, and manage deliverables. www.viroclinics.com. Kris OBrien is an Executive Director in Program Strategy, specializing in Rare Disease and Pediatrics, at Premier Research. Explore Modern RTSM Solutions. www.allucent.com. This session examines how scientific rigor can be applied to clinical outcome assessments (COAs) even though they are subjective. A significant portion of the cost in a clinical trial can be attributed to operational conduct of the trial such as site monitoring related activities, data management and site oversight. She also has a special interest in innovations that can improve the quality and efficiency of clinical trial execution. He received his medical degree (MD) and his doctoral degree (PhD equivalent) from Justus-Liebig-Universitt Giessen, Germany, and his Master of Business Administration (MBA) from the Wharton School of Business, University of Pennsylvania, PA. Kunal Sampat is the founder of the Clinical Trial Podcast, a podcast and blog platform for clinical research professionals. To understand site-side difficulties in trial recruitment and conduct, Arun served as a Senior Clinical Research Coordinator for Cardiology Phase 4 trials at the Loma Linda VA Medical Center, and as a Lead Clinical Research Specialist for Investigator-Initiated and Phase 0 3 Gastric Neuroendocrine Rare Disease trials at Stanford Cancer Center. TD2 offers fully integrated precision oncology clinical development solutions that combine the highest standards in clinical trials management, disruptive imaging, biomarker strategies, and unparalleled access to real-time patient data. TFS HealthScience is a global Contract Research Organization (CRO) that supports biotechnology and pharmaceutical companies throughout their entire clinical development journey. We are an embedded partner dedicated to the success of your study, offering managed services such as: Data Management, On-Demand Data Analytics, Biostatistics, Clinical Management, eTMF Management and Pharmacovigilance. Flexible. CISCRP staff is committed to participating and presentingspeaker, chairperson, moderator, advisor rolesin relevant and engaging educational events within the clinical research industry. Dr. Hsu is anesthesiologist and pain management physician, but also a serial entrepreneur. Our simulation-based protocol training prevents study errors, guarantees timely SIV, and frees up thousands of hours for your study team and site-staff. Fun fact: Ndidi was born and raised in Sierra Leone, and is a descendant of the Krio people who were freed slaves that returned to Freetown from Africa, America and The West Indies. actalentservices.com, To learn more , please visit our website - This talk will provide an overview of the application of Artificial Intelligence methods in clinical operations. Other companies he has founded or co-founded include: 1) IMTH, a real estate investment trust with properties through the state of California; 2) iPill Dispenser, a medical device that uses a mobile app to control a secure, stand-alone pill dispenser to prevent opioid sharing, diversion, and drug overdoses; and 3) NAOMI systems, a practice management software company that integrates digital X-rays devices in PACS, EMR and RCM billing modules. Effective management of essential clinical trial documents using eTMF solutions. www.tranquilclinicalresearch.com. Prior to SDCs inception, Richard served on the Board of Directors of Ora, Inc. (www.oraclinical.com) for over 10 years. Theyll ensure your translations will be of the highest quality, on time, and within budget. Mr. Chu has served as a mentor for the Federal Executive Board in Los Angeles, CA. Dont miss out; join us in Burlingame on March 1st& 2nd2023! To enquire about sponsorship opportunities for the conference, please contact: To enquire about speaking opportunities for the conference, please contact: Arena International is a global B2B events company for online casino players. He has worked for CROs as well as small and large biotechnology companies. Formed through the merger of IMS Health and Quintiles, IQVIA has more than 58,000 employees worldwide. Strategy/Planning: How do you make the decision to run a DCT; what are the considerations? There, he employed a broad range of methodologies, including: visual psychophysics, neuropsychological and computer-based cognitive assessments, eye tracking, electrophysiology, and structural imaging. The DIA's Digital Technology in Clinical Trials Conference discovers how digital technology is transforming the drug, device, and diagnostics development process in clinical trials. She has been with Calyx for 17 years as a key strategic leader, with a specific focus on IRT solutions. To learn more , please visit our website - www.assistek.com, To learn more , please visit our website - 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. Precision for Medicine (PFM), the full-service global CRO, is purpose-built to accelerate clinical research and development processes to bring life-changing therapeutics to those who need them most. Eurofins BioPharma Services, Laboratory Testing is a group of Eurofins companies with dedicated testing facilities for global Central Laboratory Services, Bioanalytical Services, and Specialty Virology and Oncology Services. April 18-20, 2016 Dubai, UAE. This talk will provide an overview of the application of Artificial Intelligence methods in clinical operations. Headquartered in Sydney since 1996, Novotech has come to be recognised as the CRO of choice for many US and European biotechnology firms in the Asia Pacific. www.agilexbiolabs.com. We are committed to delivering high-quality, cost-effective services according to sponsor timelines and specifications. www.gobio.com/clinical-research/. https://www.sdcclinical.com/. To learn more , please visit our website - Since 1996, ARA has supported 700+ clinical trials worldwide across all therapeutic areas. His last company, TheraSim, trained over 1 million physicians worldwide and was sold to WebMD in 2013. Currently, Audrey Funwie works in the Patient Inclusion and Health Equity team of Genentechs Chief Diversity Office. Understanding Digital and Device Safety Across a Large Organization, a Perspective of a Center of Excellence. Developing successful communication pathways in a more remote world. 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. To learn more , please visit our website - Headquartered in Uppsala, Sweden, Viedoc also has offi ces in America, France, Japan, Vietnam, and China. Prior to her work at Potrero, she was the VP of Business Development at Theranova and led marketing initiatives for C. R. Bard (now owned by Becton Dickinson), in both Shanghai and the U.S. She has also worked as a Board Fellow at the American Red Cross Bay Area, currently serves as a guest lecturer at the University of California, San Francisco and Berkeley, and spent several years in sales and training at Johnson & Johnson. https://www.medidata.com/en/clinical-trial-products/clinical-data-management/rtsm/, To learn more , please visit our website - https://www.medidata.com/. A NEW paradigm of engineering-forward analytics solutions powering digital biomarkers. He is an advisor to several biotech companies. As the Founder and Chairman, he spearheaded the ACS ProSpectives international conferences on, Process Chemistry in the Pharmaceutical Industry, and as the chair, speaker and the moderator at numerous national and international conferences on API Process Chemistry, ADCs and Drug Discovery & Development. https://www.medidata.com/, To learn more , please visit our website - Overview. About Mobile Technologies in Clinical Trials. Their experienced research team comprises key opinion leaders, board-certified cardiologists and radiologists, sub-specialty scientists, and highly trained technicians who acquire, evaluate, and report high-quality data through an efficient, cloud-based infrastructure. TORONTO, Oct. 12, 2022 (GLOBE NEWSWIRE) -- Axiom Real-Time Metrics ("Axiom"), a premier provider of unified eClinical solutions and services focused on small-to-medium life science organizations, will be exhibiting at Outsourcing in Clinical Trials New England 2022, October 12-13 in Boston, MA. The international company is a privately owned organisation which has grown organically over the past five decades now employing over 5,600 highly skilled personnel across 18 facilities including Europe, the US and Asia. http://www.mlm-labs.com. . Our collaborative approach helps maximize efficiency and agility by acting as an experienced member of your team. The 15th Annual Outsourcing in Clinical Trials New England event will bring together clinical trial professionals from big and small biopharma to uncover new technologies and processes, to optimize their clinical and outsourcing operations. Over the years, Lin has achieved success at both large corporations and startups. Company Website:https://eurofinscentrallaboratory.com/biopharma-services/, To learn more , please visit our website - From 2 to 4 November 2021. Liza Melchor-Khan is a Senior Director of Clinical Operations at NGM Biopharmaceuticals, Inc. with over 25 years of experience in the biotech and pharmaceutical industry. 4G Clinical, a leader in randomization and trial supply management (RTSM) for the global life sciences industry, is sponsoring the 2022 Outsourcing Clinical Trials DACH. ACM performs more than 20 million laboratory tests each yearspanning all medical disciplines including pathology, microbiology, molecular diagnostics, toxicology and more. These conferences closely focus on the advancements in clinical research and trials. What is critical to get right to make a digital QM System work? The 2023 programme will offer a fresh insight into the latest regulatory updates, global clinical trials, advanced technologies such as digital health and connected devices space, and more. Current topics in the Medical Device Regulatory Landscape, Presented by the FDA. From 2008 to 2011, he was Senior Clinical Trial Manager at Seattle Genetics where he was responsible for the oversight of multiple oncology clinical trials, as well as support for the development of the Clinical Operations infrastructure and regulatory authority marketing approval inspection hosting. She currently serves as Vice President of Clinical Affairs at Endogenex, a medical device company developing innovative solutions for the treatment of Type 2 diabetes. She is definitely not afraid of being the least popular girl in the room in order to support patient safety! TrialMaster, IRMS MAX, and TA Scan, the companys flagship products, lead the way in reducing complexities in the drug and device discovery and commercialization process. We atMyonexadd value to our clients by helping them always be prepared for what is next in their clinical trials. Chemistry degree from Punjab University, Institute of Chemistry, Executive Director, Global Digital Quality Management Systems and Business Intelligence BeiGene, Executive Director, Global Medical Affairs Study Management, BioMarin Pharmaceuticals, Inc. Wendi Carroll received her Pharm D from the University of the Pacific. Wed, 25 May 2022, 18:00 WebSite.
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