Confidence Pharmaceutical Research
生物技术研究
Redwood City，California 1,279 位关注者
Confidently unlocking the full potential of clinical research. Global full-service CRO you can rely on.
关于我们
Confidence Pharmaceutical Research (CPR) is a dynamic force in the pharmaceutical industry, driven by a vision to revolutionize drug development. With a dedicated team of over 100 passionate professionals, Confidence combines the global reach and full-service capabilities of a large Contract Research Organization (CRO) with the agility and client-centric focus of a boutique firm. Our lean management approach ensures cost-effectiveness without compromising on quality, making us an ideal partner for organizations seeking innovative solutions in drug discovery and clinical research.
- 网站
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https://www.confidenceresearch.com
Confidence Pharmaceutical Research的外部链接
- 所属行业
- 生物技术研究
- 规模
- 51-200 人
- 总部
- Redwood City，California
- 类型
- 私人持股
- 创立
- 2014
- 领域
- Global CRO、Clinical Trials、Regulatory Approvals、Clinical Monitoring和Medical Writing
地点
Confidence Pharmaceutical Research员工
动态
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Did you know that over 80% of clinical trials miss enrollment deadlines, and 30% experience costly delays due to retention issues? By the time these challenges are identified, it’s often too late to make quick adjustments without risking months of setbacks and budget overruns. Retention isn’t just another metric—it’s central to a study’s success. Top CRO leaders see retention as a vital investment, one that starts well before the first participant is even enrolled. It’s about designing trials with flexibility, convenience, and support in mind. Each decision, from integrating telemedicine to providing real-time support, can dramatically increase patient engagement and retention. For every dollar invested upfront in retention, studies avoid three times that in re-recruitment and timeline extensions down the road. To build a retention-focused study, set realistic enrollment goals, work with experienced sites, and design patient-friendly protocols. With these strategies in place from Day One, you’re setting up a study that’s primed for success without the costly setbacks. Ready to talk strategies for enrollment and retention? confidenceresearch.com/ #ClinicalTrials #PatientRetention #StudyEnrollment #ClinicalResearch
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Confidence is rolling its sleeves up and getting ready to tackle the elephant in the room! Stop by booth 5 today to chat with Efim Kelman, MD, MBA, Anna Ravdel, and Margaryta Mare, MD, MSc about how we can tackle your clinical research challenges together. We know it can be tough out there – from recruitment struggles and team coordination headaches to regulatory hurdles and data management concerns. At Confidence Pharmaceutical Research, we want to make your life easier. - With our incredibly low turnover rate (just 7%), our team is in it with you for the long haul? - Our lean management approach ensures efficient and quick decision-making - Our experienced CRAs and PMs are passionate and committed to your success But hey - it’s not all about work! We believe in fostering a positive and enjoyable work environment too! So bring your best questions, come by booth 5, and let’s connect! #Precision2024 #ClinicalTrials #Pharmacovigilance #DrugSafety #Biotech #Healthcare #LifeSciences #MedTech #Confidence #LetsConnect #Networking #SafetySurveillance #CostOfFailure #Workshop
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We are excited to announce that our head of Safety and Pharmacovigilance, Dr. Margaryta Mare, MD, MSc will be attending Precision in Clinical Trials Summit in San Diego next week and giving a presentation: "Clinical Trials: Cost of Safety Surveillance Fail" on Day 2, Oct 22nd, from 9:05 AM to 9:30 AM. This workshop will shine a light on the often underestimated financial and ethical implications of inadequate safety measures in clinical trials. How confident are you feeling about the safety protocols in your current clinical trials? We are curious to hear your thoughts! And are you planning on attending Precision this year? #Precision2024 #ClinicalTrials #Pharmacovigilance #DrugSafety #Biotech #Healthcare #LifeSciences #MedTech #Confidence #LetsConnect #Networking #SafetySurveillance #CostOfFailure #Workshop
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Our team is buzzing with excitement for Precision in Clinical Trials Summit 2024 in San Diego, starting next Monday! If you’re planning on attending, be sure to come by Booth 5 and say hi to our CEO, Efim Kelman, VP of Business Operations, Anna Ravdel and Head of Safety and Pharmacovigilance, Dr. Margaryta Mare, who will also be giving a workshop on “Clinical Trials: Cost of Safety Surveillance Fail” on Day 2, Tuesday Oct 22nd, from 9:05 AM to 9:30 AM. Who else is attending? We’d love to know! Drop us a line at [email protected] or let us know in the comments below. #Precision2024 #ClinicalTrials #Pharmacovigilance #DrugSafety #Biotech #Healthcare #LifeSciences #MedTech #Confidence #LetsConnect #Networking #SafetySurveillance #CostOfFailure #Workshop
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Dr. Katarina Nedman, our dedicated Medical Monitor, brings a wealth of expertise to safeguarding the integrity of our clinical trials. With a PhD in Medical Science, a background in Obstetrics & Gynecology, and extensive experience in pharmacovigilance and medical writing, she ensures our research adheres to the highest ethical and scientific standards. Her passion for patient safety and commitment to advancing medicine make her an invaluable asset to our team. To learn more about Katarina, please visit: https://lnkd.in/ezYgP8VP #Confidence #Safety #Pharmacovigilance #MedicalMonitor
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Health Tech World: Leveraging global clinical trial data: Navigating domestic regulations https://lnkd.in/d6x26hBR Having a global perspective on clinical research can be a huge benefit when seeking approval.
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Our Senior Project Coordinator, Kate, is sparking an important conversation about the skills needed to excel in Clinical Research Project Management. Do you agree that it's a blend of formal education, hands-on experience, and soft skills? Share your thoughts and experiences in the comments! #ClinicalResearch #ProjectManagement #CRO #CareerDevelopment #SoftSkills #PMTraining #Education #Experience #CareerGrowth #Pharma #Biotech #ClinicalTrials #MedTech #Healthcare
? Do You Need Formal PM Training to Excel in Clinical Research Project Management? ? As I work towards becoming a Project Manager in the clinical research field, I often reflect on what truly makes a great PM. Is formal education and certification essential, or can hands-on experience and soft skills be enough? In the CRO industry, where precision and compliance are critical, the skills required for effective project management can be nuanced. So, what helps the most? ? Formal Education: Theories and frameworks provide a solid foundation. My HR degree, for example, offered insights into organizational behavior and project management principles. Additionally, courses on modern PM methodologies have been key in refining my understanding of project lifecycles and risk management. ? Experience & Soft Skills: Real-world experience is irreplaceable, especially in the dynamic and regulated environment of clinical research. Soft skills like communication, adaptability, and problem-solving are invaluable. Whether navigating subject enrollment complexities or ensuring stakeholder alignment, these skills keep projects on track. A blend of education, experience, and soft skills seems to be the recipe for success. ? What do you think? How important has education been in your PM journey? What training has been the most helpful? ?? I’ve noticed a lack of specific training for project management in clinical research. Courses like those offered by CCRPS and ECCRT are available — any feedback on those? General PMI-CAPM and PMP training and certification also seem like appropriate options, but I’d love to hear your advice. #ProjectManagement #ClinicalResearch #CRO?#SoftSkills #CareerGrowth ?
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We are thrilled to invite you to meet Dr. Tatiana Dumpis, Medical Director at Confidence. With specialty certifications in anesthesiology, intensive care, and medical oncology, Dr. Dumpis has a proven excellent record of more than 20 years of experience as both a clinician and clinical researcher. Her extensive experience combined with her academic teaching background and over 8 years of medical monitoring in I-IV phase clinical trials, provides a unique perspective to her role as Medical Director. In her exciting role, Dr. Tatiana Dumpis is responsible for protocol design, therapeutic training, and medical monitoring, ensuring the highest standards of patient safety, data integrity, and ethical conduct throughout your clinical trials, ultimately leading to regulatory approvals and the best possible trial outcomes. Tatiana's dedication to medical excellence and vast professional experience make her an invaluable member of the Confidence team. https://bit.ly/46swk5n #Confidence #MedicalDirector #SafetyManagement #GlobalCRO #ClinicalTrials #Oncology #MedicalMonitoring
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Thrilled to connect with our valued clients in the heart of New Orleans! Building long lasting relationships is at the core of our commitment to clinical research excellence. #ConfidenceCRO #ClinicalResearch #Partnerships #NewOrleans
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