Data Management & Statistics Jobs in Life Sciences’ Post

Safeguarding compliance and extracting actionable insights from data, Clinical Data Managers play an essential role in preserving data integrity and medical advancement. https://hubs.ly/Q025hcLK0 Cristina Moore, CCDM #clinicaltrial #datamanagement #drugdevelopment

As a seasoned Data Manager with more than 16 years of Data management experience for small Clinical Research Organizations (CROs), I bring a wealth of experience and a tailored approach to each project. I am offering my expertise in streamlining clinical trials, enhancing data integrity, and ensuring regulatory compliance, all while maintaining a keen eye on budget constraints and timelines. I am passionate about empowering CROs to maximize their potential through strategic planning and innovative solutions. Let's connect and explore how I can support your organization in achieving its goals and advancing medical research. Together, we can drive healthcare forward. #ClinicalResearch #CROConsulting #InnovationInHealthcare

🌟 Exploring the world of Clinical Research and Clinical Data Management (CDM)🌟 I wanted to share My understanding into the dynamic fields of Clinical Research and Clinical Data Management (CDM) 🧬 These domains plays a crucial role in advancing medical science and ensuring the safety and efficacy of new treatments Clinical Research involves conducting trials to evaluate Medical,surgical,or behavioural interventions. it's all about discovering new ways to improve patient care and health outcomes..💊🩺 On the other hand, CDM focuses on the Collection, Cleaning, and management of data from Clinical trial. The data should be Accurate and reliable because it is a backbone of the Clinical Research to ensure that the findings are credible and actionable.🔍📂 As I dive deeper into these areas I'm also dedicated to expanding my skills set.. Learning new techniques and tools is essential for staying ahead in this ever-evolving industry..🚀📚 Excited to connect with industry professional and share insights in this dynamic field.😊 🌟Thought🌟:- Embrace every Challenge as an opportunity to grow,learn, and evolve. Keep pushing forward with Courage and determination..Every single efforts Counts 🧬Stay updated with more information on clinical research and CDM domain and the work flow of the Clinical trails..🧬 #ClinicalResearch #Clinicaldatamanagement #Continuouslearning #HealthcareInnovation

The responsibilities of a clinical data manager are becoming increasingly complex and demanding... As clinical research and clinical data management continue to evolve and innovate, the demands on professionals in this field increase. The role of a clinical data manager has become more complex, requiring a constantly changing skill set to keep pace with cutting-edge technology. One of the key challenges is staying abreast of these changes while also understanding developments in other organisations. This is where the Association for Clinical Data Management (ACDM) plays a crucial role, offering support and resources to help the sector to navigate this dynamic landscape. For over 35 years, the ACDM has been at the forefront of the global clinical data management community, supporting it through a period of continuous change. The ACDM facilitates this support through various initiatives, including Data Management Expert Groups, Hot Topics discussions, Symposium Events, and the Annual Conference. These activities provide valuable opportunities for professionals to stay updated on industry trends, share knowledge, and enhance their skills, ensuring they are well-equipped to meet the ever-evolving demands of the sector. Find out more about the ACDM here: https://acdmglobal.org/ Robert King, Sverre Bengtsson, Jo Marshall, Nina Reyes, Eva Alder, Amelie Spieser, Anita Kratchmarov, Nicola Götz, Ashley Howard, Richard Davies #clinicaltrials #clinicalresearch #clinicaldatamanagement #acdm

Are the entry requirements for a new clinical data manager becoming more specific and more challenging than they used to be........ There has never been a more interesting time to work in clinical data management. The role has changed considerably over the last two decades and more so over the last few years. These changes have not only created a difference in the day-to-day tasks of a clinical data management, but have also created new roles and new career paths. These are great opportunities if you are already in a CDM role but what if you are looking to get into the industry. Have the entry requirements become more specific and more challenging? We asked this question in a recent ACDM LinkedIn Poll. The results were (N=142): Yes: 81% No: 19% It will be interesting to explore these results further. How have the criteria changed and is this consistent across regions and companies? Robert King, Sverre Bengtsson, Nina Reyes, Jo Marshall, Eva Alder, Anita Kratchmarov, Amelie Spieser, Nicola Götz, Ashley Howard, Richard Davies #clinicaltrials #clinicalresearch #clinicaldatamanagement #acdm

Meet Leonette Yeadon Peebles, CCDM. Leonette is a Principal Clinical Data Scientist with Syneos Health and we are honored that she authored an article for the premiere issue of Interim Visits magazine. Please read Leonette's article "The Importance of Clean Data in Clinical Trials" by visiting our website! #clinicalresearch #clinicaltrials #clinicaldatamanagement #syneoshealth #clinicalresearchassociates #clinicalprojectmanagement

📊 Elevating Clinical Data Validation Skills 🚀 In the dynamic realm of clinical research, refining your data validation skills is a game-changer. Here's a quick roadmap to enhance your prowess in ensuring data accuracy and integrity: 🤓 Deep Dive into Standards: Immerse yourself in industry standards and regulatory requirements governing clinical data. A strong foundation is key! 🛠️ Hands-On with Tools: Get hands-on experience with data validation tools and software used in clinical research. Proficiency in these tools enhances efficiency. 🕵️ Attention to Detail: Sharpen your attention to detail. Uncover discrepancies, outliers, and nuances within datasets that could impact data quality. 🤝 Collaboration is Key: Engage with colleagues and cross-functional teams. Collaborate on data validation processes, share insights, and learn from diverse perspectives. 🚦 Stay Informed: The clinical landscape evolves. Regularly update your knowledge on emerging trends, technologies, and best practices in clinical data validation. Continuous improvement in clinical data validation is not just a skill—it's an investment in ensuring the reliability and success of clinical research endeavors. Let's excel together! 💡🌐 #ClinicalDataValidation #DataIntegrity #continuouslearning #validation #linkedincommunity #linkedinfollowers #clinicaltrials #clinicaldatamanagement

Managing Change In Clinical Trials: The Data Management Playbook Source: OpenClinica https://lnkd.in/eyE2zdB4 Dealing with changes in clinical trials can be tough because there are so many different people involved, each with their own way of doing things. But if we plan ahead for changes, especially related to the data needed for therapy submissions, we can save time and money in the long run.

Close your eyes for one moment. Now imagine... that you are a clinical data professional who is put in charge of a pivot, phase 3 clinical study that has been going on for 2 years. You’re excited, but nervous.  😎 😅 Are there data integrity issues lurking in your audit trail? 🙈 Do the right personnel have the correct permissions to manage data? 💁🏽♂️ Is special handling required for certain categories of data? ✍🏽 The trial team has had a lot of turnover. The protocol has been amended n times.  You get a slack message - “Hi, we have an analysis in 3 months. Can we lock data in 8 weeks?”. 😵 The plot thickens… Okay, time to snap out of it. If I were you, the first thing I would be looking for is the Clinical Data Management Plan (CDMP). Hoping that it contains all the data storytelling a good clinical study deserves. So I can ramp up quickly. So I can paint a good picture for that next audit. There are MANY categories of information I’ll want to get acquainted with, but here are 5 important items a good CDMP should contain: 1️⃣ Systems used for the trial (incl., validation, user access management) 2️⃣ Roles and permissions (who can do what with the study data) 3️⃣ Data categories and sources (by eCRF, method of capture) 4️⃣ Data quality approaches  5️⃣ Special data handling This is not an exhaustive list, but will help you get started on your journey to successfully manage that pivotal, phase 3 study. Which categories are the most important for you as a clinical data professional? Share below! #clinicaldatamanagement #clinicaltrials #clinicaloperations #realworldevidence #research