Amaan Ansari’s Post

Want to pursue a career in Clinical Data Management? 🚀 Explore the key job roles in CDM and how you can get started! Full video on LLRI's YouTube. 🔗 https://lnkd.in/gbDgbtZH #ClinicalDataManagement #CDM #ClinicalTrials #ClinicalResearch #ClinicalData #DataManagement #HealthcareData #ClinicalDataAnalytics #ResearchDataManagement #PharmaData #MedicalDataManagement #RegulatoryCompliance #ClinicalStudyData #DataIntegrity #ClinicalTrialManagement #DataQuality #HealthTech #ClinicalResearchOrganization #PharmaceuticalResearch #DataManagementSolutions

𝐃𝐚𝐭𝐚 𝐌𝐚𝐧𝐚𝐠𝐞𝐦𝐞𝐧𝐭 𝐏𝐥𝐚𝐧 𝐎𝐯𝐞𝐫𝐯𝐢𝐞𝐰📚 •A data management plan ensures compliance with good clinical data management •practices throughout the entire clinical trial, •Data Management plan is a document which defines all data management activities, to promote consistent, efficient and effective data management practices for each individual study. •Data management plan not only describes data management activities, but also provide an agreement among all parties concerning responsibilities and deliverables related to clinical data management. 𝐎𝐛𝐣𝐞𝐜𝐭𝐢𝐯𝐞𝐬 •After completing this training you will be able to: •Understand how a Data Management Plan is created in compliance with good clinical data management practices. •Describe all study specific data management activities, roles and responsibilities. •Understand how DMP acts as central reference for the supporting documentation and processes used during the life cycle of the study. 𝐃𝐌𝐏 𝐂𝐨𝐦𝐩𝐨𝐧𝐞𝐧𝐭𝐬 DMP Components vary from 1 study/client to another. On a broader level, information on the following areas need to be collected within the DMP: -Data Flow -Data Capture -Study Setup -Data Entry -Data Transfer -Data Processing/ Management -Coding -Safety Data (Serious Adverse Events) -External data -Any milestones if applicable or -Database Lock and Unlock process -Archival of Clinical Data -Reports -Quality Shaikh Aqdus Mateen Bagwan PharmaWiz Anas Tarique #clinicaldatamangement #cdm #clinicalresarch

: 🌟 Hello, I’m Swathi Suseela – Clinical Data Management Enthusiast! 🌟 I am passionate about making a meaningful impact in healthcare through Clinical Data Management (CDM). With a strong foundation in this dynamic field, I’ve developed a deep understanding of how vital accurate, high-quality data is in driving clinical research forward. 💡 My journey into CDM started with a fascination for data and its potential to shape patient outcomes. As I’ve progressed, I’ve honed my skills in data collection, validation, and ensuring compliance with the highest industry standards. My goal is to share what I’ve learned with others in the field, helping to build a community of like-minded professionals who are passionate about advancing CDM together. I believe in continuous learning, collaboration, and always striving for excellence. ✨ Let’s connect and exchange insights on Clinical Data Management! ✨ What’s your journey in CDM? I’d love to hear your story and collaborate on our shared goals. 🚀 #ClinicalDataManagement #CDM #DataDriven #HealthcareInnovation #Collaboration #DataQuality #ClinicalResearch

Top 10 Companies Actively Recruiting Clinical Data Management Specialists #clinicaldatamanagement #careeropportunities #biotechnologyjobs #pharmajobs #lifesciencecareers #datamanagement #healthcarejobs #clinicalresearch #jobsearch #careergrowth #clinicaldata #biotechcareers #pharmaceuticalindustry #jobopportunities #cdmjobs

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

Want to understand data management as a clinical researcher? Then this course is for you! We will delve into data management terminology, plans, coding and (e)CRFs so that you can work seamlessly with data management professionals. The course outlines the common terms and process for data management and how to work effectively with your data manager. Need more information? Click the link below! https://lnkd.in/eRkskkgs #clinicalresearch #clinicaltrials #patients #weareclinicalresearch #clinicalresearchassociate #graduate #career #data #datamanagment #theICR

Just completed a course on ✨️"Clinical trials Data Management and Quality Assurance".✨️ I am excited to implement my new skills and take my future career to the next level. A small step👣 towards my goals. 🎯 #clinicalresearch #qualityassurance #datamanagement #clinical trial

🚀Day 32 : Mastering Clinical Data Management🚀 🔐 Database Lock: A Critical Milestone in Clinical Data Management 🔐 As we reach the final stages of a clinical trial, ensuring data accuracy and integrity becomes paramount. One of the key responsibilities during the closeout phase is achieving a successful Database Lock (DBL). Here’s why it’s so crucial: 📊 Final Data Review: All data must be reviewed, queries resolved, and discrepancies addressed. A clean dataset is the foundation for accurate analysis and regulatory submissions. ✅ Pre-Lock Activities: Rigorous validation checks are performed, listings reviewed, reconciliation activities, Final QC and any outstanding data management tasks are completed. Time management and attention to detail are critical during this phase. 🔒 Database Lock: Once locked, the data becomes immutable, meaning no further changes can be made. This ensures the integrity of the clinical trial data, paving the way for statistical analysis and submission to regulatory authorities. 🌟 At this point, collaboration across teams—data management, clinical operations, and biostatistics—is key to ensuring the database is locked accurately and on time. 🚀 Achieving a successful Database Lock is a major step toward clinical trial success and bringing new, safe, and effective therapies to patients. #ClinicalDataManagement #DatabaseLock #ClinicalTrials #DataIntegrity #Teamwork #HealthcareInnovation #DataDrivenResearch #closeout #datalock #lock #data #cdm #day32

A small CRO is turning their data associates into… well, everything. Okay, not literally everything. I came across a Reddit post where someone shared their journey from clinical data associate to a potential role blending data management, programming, and stats. The manager asked them if they could learn R and hinted at “easy” stats tasks like creating data and safety monitoring boards (DSMB)/interim analysis tables. In 2024, when efficiency is king and time is money, is this the best approach? Consider: 1. Time investment in learning new skills. 2. Potential for diluted expertise. 3. Learning curves slowing down project timelines. 4. More room for error as a new, inexperienced team member. The alternative is leveraging purpose-built tools that actually support the entire clinical trial ecosystem, like #studyOS.  A tool that: • Gives CRAs instant access to site performance, with metrics like query rates, data completeness, and protocol deviations. • Provides executives with clear, actionable insights they can trust. • Eliminates the need for manually swapping Excel files just to track out-of-window visits—because who’s got time for that? • Allows medical monitors to easily track and review safety data. The future is about tools that do more, enhancing the entire team’s performance and speeding up the path to market. #ClinicalTrials #ClinicalResearch