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Why do Indian #Biostatisticians lack strong expertise and specialization in specific therapeutic areas? – This could be due to the broad exposure on general biostatistics rather than concentrated projects in niche therapeutic fields, which can limit their in-depth exposure and expertise. Let us know your experience or view on this. --------------- Greetings! I'm Dr Nirali Mehta ✨, Founder and CEO of PHARMA-STATS. Follow me for regular content aimed at helping you overcome challenges and elevate your knowledge in your biostatistics and programming career. #biostatistics #NiraliTalks #pharmastats #clinicaltrials #Pharmaceuticals #career #jobs #clinicalresearch #CLinicaldatamanagement #medicalwriting #cliniops #rstats #biostatisticiandiary #statisticalprogramming

🌐 Bridging Pharmacology and Technology 🩺💻 I asked #ChatGPT to “draw a picture of my life,” and this image beautifully captures my dual focus on pharmacology and technology. From diving deep into drug safety to exploring tech innovations, I’m passionate about using #AI to enhance our understanding of healthcare. The synergy between #pharmacology and #technology holds immense potential to transform patient care and data-driven decision-making. Excited about the future of healthcare at the intersection of these fields! #Pharmacology #HealthcareInnovation #AIinHealthcare #TechForGood

Clinical Pharmacology is crucial in statistical programming, specifically in analyzing data from clinical trials and PK/PD studies utilizing SAS or R. #ClinicalPharmacology #StatisticalProgramming #ClinicalResearch

Why Choose MD Pharmacology as Your Medical Specialty? Recently, I've been receiving numerous inquiries from doctors considering MD Pharmacology as a specialty. Here’s why you should consider it: ✅Diverse Career Opportunities: i) Clinical Research: Dive into cutting-edge studies and trials. ii) Medical Writing: Craft compelling and accurate medical content. iii) Medical Advisor: Provide expert advice and guidance in the pharmaceutical industry. iv) Pharmacovigilance: Ensure drug safety and efficacy. v) Clinical Practice: Apply your knowledge directly in clinical settings. vi) Domain Expert: Become a specialist in pharmacology-related fields. vii) Healthcare AI: Integrate pharmacological expertise with artificial intelligence. viii) Drug Discovery: Contribute to the development of new medications. Ix) Biostatistics: Apply statistical methods to medical research. x) Medical Startup Advisor: Guide innovative medical startups with your expertise. ✅Flexibility and Variety: Combine various roles and avoid monotony by applying your pharmacology knowledge across multiple areas. ✅Enduring Clinical Knowledge: Despite being considered a para-clinical branch by some, your clinical knowledge remains valuable and applicable across many domains. Embrace MD Pharmacology with an open mind, and seize the many opportunities available in the right place and time. The field is vast, and your career can be as dynamic and varied as you choose! #MDPharmacology #MedicalCareer #Pharmacology #ClinicalResearch #HealthcareAI #DrugDiscovery #Medicine #Healthcare #Clinicalpractice

𝑾𝒆 𝒂𝒓𝒆 𝒉𝒊𝒓𝒊𝒏𝒈 𝒉𝒆𝒓𝒆 𝒂𝒕 𝑫𝒂𝒚 𝑶𝒏𝒆! Both of these roles are 𝘣𝘳𝘢𝘯𝘥 𝘯𝘦𝘸 𝘩𝘪𝘳𝘦𝘴 to support our important mission. 𝐀𝐬𝐬𝐨𝐜𝐢𝐚𝐭𝐞 𝐃𝐢𝐫𝐞𝐜𝐭𝐨𝐫, 𝐁𝐢𝐨𝐬𝐭𝐚𝐭𝐢𝐬𝐭𝐢𝐜𝐬 🟡 PhD in Biostatistics or Statistics required 🟡 5+ years experience in biotech with Sponsor experience 🟡 Hands-on design and analysis of both early and late phase oncology trials 🟡 Proven background interacting with Health Authorities for regulatory submissions 𝐒𝐞𝐧𝐢𝐨𝐫 𝐌𝐚𝐧𝐚𝐠𝐞𝐫, 𝐂𝐥𝐢𝐧𝐢𝐜𝐚𝐥 𝐏𝐡𝐚𝐫𝐦𝐚𝐜𝐨𝐥𝐨𝐠𝐲 🟡 PharmD or PhD in Pharmaceutical Sciences required 🟡 Experience leading the design, execution, and interpretation of clinical drug-drug interaction studies 🟡 Proficiency with Phoenix WinNonlin 🟡 Proven background drafting Clinical Pharmacology responses to support regulatory interactions If you do not see anything you fit and are interested in joining us, make sure to apply to the Our Communities you are interested in and follow the Day One page here on LinkedIn. We search there for those that have indicated interested in us when we open new roles! 𝐎𝐮𝐫 𝐌𝐢𝐬𝐬𝐢𝐨𝐧 𝘐𝘯𝘴𝘱𝘪𝘳𝘦𝘥 𝘣𝘺 𝘵𝘩𝘦 𝘶𝘳𝘨𝘦𝘯𝘵 𝘯𝘦𝘦𝘥𝘴 𝘰𝘧 𝘤𝘩𝘪𝘭𝘥𝘳𝘦𝘯 𝘸𝘪𝘵𝘩 𝘤𝘢𝘯𝘤𝘦𝘳, 𝘋𝘢𝘺 𝘖𝘯𝘦 𝘤𝘳𝘦𝘢𝘵𝘪𝘷𝘦𝘭𝘺 𝘢𝘯𝘥 𝘪𝘯𝘵𝘦𝘯𝘵𝘪𝘰𝘯𝘢𝘭𝘭𝘺 𝘥𝘦𝘷𝘦𝘭𝘰𝘱𝘴 𝘯𝘦𝘸 𝘮𝘦𝘥𝘪𝘤𝘪𝘯𝘦𝘴 𝘧𝘰𝘳 𝘱𝘦𝘰𝘱𝘭𝘦 𝘰𝘧 𝘢𝘭𝘭 𝘢𝘨𝘦𝘴 𝘸𝘪𝘵𝘩 𝘭𝘪𝘧𝘦-𝘵𝘩𝘳𝘦𝘢𝘵𝘦𝘯𝘪𝘯𝘨 𝘥𝘪𝘴𝘦𝘢𝘴𝘦𝘴. 𝐉𝐨𝐢𝐧 𝐔𝐬!🎗💛 #clinicalpharmacology #biostatistics #oncology 

Clinical Pharmacology

⚡Accelerating Safety Pharmacology Starts at Attentive Science! ⚡ As the Safety Pharmacology Society (SPS) meeting approaches, the spotlight on safety pharm intensifies! At Attentive Science, we’re proud to offer the agility that gets your studies off the ground quickly, without compromising quality. While AI is transforming our field, it’s clear that safety pharmacologists will continue to make critical decisions. Our agility, personal attention, and streamlined processes help you stay ahead. Don’t let your project get stuck in a queue. Together we can accelerate your safety pharmacology studies! 🚀 Read More➡️🔗https://lnkd.in/drKkG8Br   #SafetyPharmacology #DrugDevelopment #AI #NonClinical #2024SPS

Dear LinkedIn Family, I have completed my Master of Pharmacy in Pharmacology & also completed my Post Graduate Diploma in Clinical Data Management. I am looking to start my career in CDM. Hence, I have started learning the basics that are required for CDM. Thanks #AmaanAnsari for your guidance. 🔬💊Today I would like to share some basic insights into the fascinating world of Drug Discovery and Development! 💊🔬 As a cornerstone of modern healthcare, Drug Discovery and Development play a pivotal role in improving and saving lives. Here are some fundamental concepts to get you started: Understanding Disease Biology: It all begins with comprehending the biological mechanisms underlying diseases. Researchers delve into intricate pathways and molecular interactions to identify potential targets for intervention. Target Identification and Validation: Once a promising target is identified, rigorous validation processes ensue to ensure its relevance and feasibility for drug development. This involves a blend of in vitro and in vivo experiments, as well as computational modeling. Preclinical Development: Before human trials commence, candidate compounds undergo extensive preclinical testing to evaluate safety, pharmacokinetics, and efficacy. This stage typically involves animal studies and toxicity assessments. Clinical Trials: The most critical phase involves testing the potential drug in human subjects through carefully controlled clinical trials. These trials progress through phases, from assessing safety (Phase I) to efficacy and side effects (Phases II and III). Regulatory Approval: Successful completion of clinical trials paves the way for regulatory approval. Health authorities meticulously review data to ensure the drug's safety and efficacy before granting marketing authorization. Post-Marketing Surveillance: Even after approval, drug safety remains a top priority. Continuous monitoring through post-marketing surveillance helps detect any adverse effects and ensures ongoing safety evaluation. Join me in exploring the dynamic of Drug Discovery and Development, where science and innovation converge to transform healthcare! 💡💼 #DrugDiscovery #Pharma #Biotech #HealthcareInnovation #Science Feel free to share your thoughts and insights! Let's keep the conversation going. ✨

Ready to explore the fascinating world of pharmacology 💊? Check out our latest video on Paracetamour where we break down our first topic General Pharmacology—what it is, its different branches, and its associated biological factors. 🎥 Watch the video and dive into the science with us! If you’re curious and want to learn more, don’t forget to subscribe for more exciting content! 🚀 Your journey into pharmacology starts now! 💊✨

Novartis is hiring for the position: Principal Scientist - Toxicology Location: Hyderabad Follow MEDBOTS.IN: Healthcare, Pharma, hospital Jobs & internships India -Design and implement the early safety screening & profiling strategies, including those associated with secondary pharmacology, genetic toxicology and cardiovascular safety, in collaboration with internal and external partners. -Give to early ADME-Tox data unification, harmonization, curation, and augmentation to support the Predictive Safety Strategy -Effectively communicate with customers, including experimental design, data quality, timeline requirements and flowchart planning. -Understand and implement agreed business strategy defined by local and global Preclinical Safety Profiling requirements, help to lead budget, ensuring appropriate coordination of projects. Please check the comments for the link to apply. #criticalcare #pharmaceutical #generalmedicine #medicine #neurologist #md #mbbs #healthcare #medicaladvisor #medicaljobs #medicalofficer #cardiologist #bhms #bams #healthcarejobs #nutrition #doctorjobs #pharmacist #pharmacistjobs #pediatric #physiotherapist #sales #pharma #drugsafety #drug #drugsafetyassociate #clinicaldatamanagement #scientificwriting #medicalinformation #patientcare #occupationaltharapist #senior #scientificwriting #manager #regulatoryaffairs #head #dataanalytics #pharma