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#hiring Senior Director, Medical Affairs, San Jose, United States, fulltime #jobs #jobseekers #careers #SanJosejobs #Californiajobs #ExecutivePositions Apply: https://lnkd.in/dw3rBcaB ABOUT THE TEAM The external partnerships team within Visby Medical has had a pivotal role in the evolution of this technology: it has succeeded in obtaining 80 million dollars in non-dilutive funding from federal grants and contracts, appointed the company's scientific advisory board, represented Visby Medical at various federal agencies including the CDC, BARDA, NIH and the DoD, participated in negotiations with the pharmaceutical industry and initiated research projects with academic partners to evaluate the performance features of the Visby device and quantify its cost effectiveness. ABOUT THE JOB Visby Medical now seeks a Ph.D. scientist or M.D. physician scientist who will lead the external partnerships team as it seeks to accomplish the following objectives; HOW YOU'LL MAKE AN IMPACT Successfully compete for relevant grants and contracts from US Federal agencies including NIH, DoD, BARDA, CDC, from NGOs including the Bill and Melinda Gates Foundation and the Wellcome Trust and from public-private partnerships including CarbX. The resulting funds would be used to augment Visby Medical's R&D budget, fund high yield-high risk innovation projects, expand Visby Medical's product pipeline and support the use of the Visby device in settings where rapid molecular diagnostics are not currently available, including underserved populations. Initiate collaborations with the pharmaceutical industry to support deployment of the Visby platform as a companion/complementary diagnostic for emerging new antivirals or to expedite clinical trials of new antimicrobials. Initiate research partnerships with academic partners to carry out studies of the performance features and medical economics of the visby platform. Provide leadership to a talented team of external partnership scientists within Visby Medical. Be the Visby scientific and technical representative to agencies of the federal government. Participate in meetings of the technical, clinical trial and commercial teams within Visby, seeking synergies between the activities of the external partnership group and the missions of other groups within Visby. ON YOUR FIRST DAY WE'D LIKE YOU TO HAVE MD or PhD degree with a focus in infectious diseases; experience conducting multidisciplinary research projects; experience writing and managing research projects funded by external agencies, including agencies of the US federal government. Experience publishing the results of these projects in peer-reviewed journals. Experience presenting research findings to scientific and medical audiences. Prior work in or with USG agencies, foundations or public private partnerships in the areas of grants management, advocacy, policy development etc. Experience working i

#hiring Senior Director, Medical Affairs, San Jose, United States, fulltime #jobs #jobseekers #careers #SanJosejobs #Californiajobs #ExecutivePositions Apply: https://lnkd.in/dw3rBcaB ABOUT THE TEAM The external partnerships team within Visby Medical has had a pivotal role in the evolution of this technology: it has succeeded in obtaining 80 million dollars in non-dilutive funding from federal grants and contracts, appointed the company's scientific advisory board, represented Visby Medical at various federal agencies including the CDC, BARDA, NIH and the DoD, participated in negotiations with the pharmaceutical industry and initiated research projects with academic partners to evaluate the performance features of the Visby device and quantify its cost effectiveness. ABOUT THE JOB Visby Medical now seeks a Ph.D. scientist or M.D. physician scientist who will lead the external partnerships team as it seeks to accomplish the following objectives; HOW YOU'LL MAKE AN IMPACT Successfully compete for relevant grants and contracts from US Federal agencies including NIH, DoD, BARDA, CDC, from NGOs including the Bill and Melinda Gates Foundation and the Wellcome Trust and from public-private partnerships including CarbX. The resulting funds would be used to augment Visby Medical's R&D budget, fund high yield-high risk innovation projects, expand Visby Medical's product pipeline and support the use of the Visby device in settings where rapid molecular diagnostics are not currently available, including underserved populations. Initiate collaborations with the pharmaceutical industry to support deployment of the Visby platform as a companion/complementary diagnostic for emerging new antivirals or to expedite clinical trials of new antimicrobials. Initiate research partnerships with academic partners to carry out studies of the performance features and medical economics of the visby platform. Provide leadership to a talented team of external partnership scientists within Visby Medical. Be the Visby scientific and technical representative to agencies of the federal government. Participate in meetings of the technical, clinical trial and commercial teams within Visby, seeking synergies between the activities of the external partnership group and the missions of other groups within Visby. ON YOUR FIRST DAY WE'D LIKE YOU TO HAVE MD or PhD degree with a focus in infectious diseases; experience conducting multidisciplinary research projects; experience writing and managing research projects funded by external agencies, including agencies of the US federal government. Experience publishing the results of these projects in peer-reviewed journals. Experience presenting research findings to scientific and medical audiences. Prior work in or with USG agencies, foundations or public private partnerships in the areas of grants management, advocacy, policy development etc. Experience working i

🔬 About Karius: Karius is a venture-backed life science startup revolutionizing the way pathogens and microbes are observed in the body. Our innovative approach unlocks valuable information from microbial cell-free DNA, enabling doctors to solve complex cases, accelerating clinical trials, discovering new microbes, and reducing patient suffering globally. Join us in our mission to conquer infectious diseases through genomic sequencing and machine learning. #LifeScience #Innovation #MedicalResearch #Pathogens 🔍 Position Summary: We're seeking an exceptional Medical Science Liaison (MSL) to join our team and support our commercial efforts. As an MSL, you'll collaborate with clinical sales managers, develop strategies to boost sales, educate healthcare professionals about our products, and establish strong relationships with key opinion leaders. Join us in making a significant impact on patient care and global health. #MedicalScienceLiaison #HealthcareSales #ClinicalUtility #PatientCare 💼 Why Join Us? At Karius, we're at the forefront of infectious disease diagnostics, leveraging advanced technologies and groundbreaking solutions. Our comprehensive test identifies over a thousand pathogens directly from blood, empowering physicians to deliver better care to previously untreated patients. Join our team and witness firsthand the life-changing impact of your work at scale. #InfectiousDisease #GenomicSequencing #LifeChangingWork 🌟 Primary Responsibilities: - Provide clinical expertise to support sales and marketing activities. - Deliver presentations and training sessions to healthcare professionals. - Foster collaboration with key opinion leaders and develop relationships with clinicians. - Stay updated on clinical advancements and provide input to business development. - Collaborate with advisors and business partners to drive success. #ClinicalExpertise #HealthcareEducation #Collaboration 🎉 What's Fun About the Job? Working at Karius means embracing new challenges and opportunities in the field of infectious disease diagnostics. You'll have the chance to tap into cutting-edge technologies, innovate where current solutions fall short, and witness the significant impact your work has on people's lives. Join us in shaping the future of healthcare. #Innovation #CuttingEdgeTechnology #FutureOfHealthcare 🌍 Travel: This role requires up to 70% travel, both locally and regionally. #TravelOpportunities #GlobalReach 💼 Position Requirements: - Bachelor's degree in Nursing, Physician Assistant Studies, or licensed Pharmacist. - Clinical advanced degree preferred. - Measurable experience as a clinician or nurse. - Familiarity with infectious disease diagnosis and treatment. - Valid Driver's License. - Proficiency in Microsoft Office and contact management databases. - Knowledge of medical institution hierarchy. - Sales experience and knowledge of laboratory workflow, a plus. - Familiarity with cfDNA technology, a plus...

🔬 **Experienced Medical Professional with a Passion for Innovation, Research and Strategic Solutions** 🔬 Greetings, LinkedIn community! I'm thrilled to share insights into my professional journey and aspirations with you. With a robust background in hematology, oncology, and a wealth of clinical experience, I'm driven by a relentless pursuit of excellence and innovation in healthcare. **Professional Journey:** Throughout my tenure as a Junior Clinical Fellow in Oncology and Hematology, I've had the privilege of providing specialized care to patients grappling with complex cancer and blood disorders. From conducting meticulous patient assessments to formulating tailored treatment plans, my commitment to delivering compassionate, patient-centered care remains unwavering. As a firm believer in the power of teamwork, I've had the honor of collaborating with multidisciplinary teams to ensure integrated and holistic care for patients. Whether leading clinical teams, mentoring junior staff, or participating in collaborative research endeavors, fostering a culture of continuous learning and professional development has always been at the forefront of my endeavors. Driven by a passion for innovation, I'm deeply invested in exploring new frontiers in healthcare. From exploring emerging technologies to spearheading research initiatives, I'm committed to pushing the boundaries of medical science to enhance patient outcomes and quality of life. **Future Pursuits:** As I embark on the next phase of my career journey, I'm eager to explore opportunities that allow me to leverage my medical expertise in roles that promote innovation and impact. Whether it's contributing to translational research, driving product development, or exploring new therapeutic modalities, I'm excited about the possibilities that lie ahead. **Let's Connect:** If you share my passion for innovation and are interested in exploring collaboration opportunities or simply connecting with like-minded professionals, I'd love to hear from you! Let's join forces to drive positive change and make a meaningful difference in the lives of patients worldwide. #HealthcareInnovation #MedicalResearch #Oncology #Hematology #ProfessionalDevelopment #Collaboration #InnovationInHealthcare #MedicalLeadership #HealthcareImpact #ManagementConsultancy

A Complete Guide of 𝐏𝐨𝐢𝐧𝐭-𝐨𝐟-𝐜𝐚𝐫𝐞 𝐃𝐢𝐚𝐠𝐧𝐨𝐬𝐭𝐢𝐜𝐬 [PDF Guide] Point of care testing is a type of medical diagnostic testing done near to the patient's location of care, away from the clinical laboratory. #Pointofcare testing helps patient, doctor, and care team to receive the results quickly, which enables them to make better urgent clinical management decisions. The Latin America region has noted significant epidemiological burden of infectious diseases in the recent years. The increased prevalence of #infectiousdiseases have led to a greater demand for PoC diagnostics technologies in the region. 𝐂𝐥𝐢𝐜𝐤 𝐡𝐞𝐫𝐞 𝐟𝐨𝐫 𝐏𝐃𝐅 𝐆𝐮𝐢𝐝𝐞 👉 https://lnkd.in/dQ69nS8r Owing to the rapid increase in the geriatric population, chronic diseases are becoming a major health problem in #LatinAmerica. As a result, the demand for diagnostic products and services is increasing in the region. For instance, in 2019, Alere Inc. (U.S.) launched its ID NOW point of care molecular platform in Brazil with tests for the rapid detection of respiratory diseases, such as influenza, bronchiolitis, and pharyngotonsillitis. Apart from such developments from #PoC #diagnostics tests providers, conferences and workshops to create awareness among local medical device manufacturers and healthcare community are also supporting the growth of the PoC diagnostics market in Latin America. 𝐃𝐫𝐢𝐯𝐞𝐫𝐬: 1. Increasing Prevalence of Infectious Diseases along with the Growing Geriatric Population 2. Increasing Initiatives by Manufacturers 3. Shortage of Skilled Laboratory Technicians 4. Increasing Funding/Investments for the Development of PoC Products 5. COVID -19 Impact Assessment 𝐊𝐞𝐲 𝐏𝐥𝐚𝐲𝐞𝐫𝐬: Alere Inc. (U.S.), F. Hoffmann-La Roche Ltd (Switzerland), Danaher Corporation (U.S.), Thermo Fisher Scientific (U.S.), Becton, Dickinson and Company (U.S.), Quidel Corporation (U.S.), biomérieux S.A. (France), Chembio Diagnostics (U.S.), Johnson & Johnson (U.S.), Siemens Healthineers GmbH (Germany). #rapidtesting #rapidtest #poct #pocus #medicalequipment #medicaldevices #medicaldevice #medicaldevicesales #meddevice #patientcare #healthcare #healthtech #biotechnology #hospitals #microfluidics #moleculardignostics #homecare #homehealthcare #tech #technology

#hiring *Medical Science Liaison (MSL) Solid Tumor Oncology Washington, DC*, Washington, *United States*, fulltime #jobs #jobseekers #careers #Washingtonjobs #DistrictofColumbiajobs #HealthcareMedical *Apply*: https://lnkd.in/graABVMB About the roleThe Medical Science Liaison (MSL) role is a field based, customer-facing, non-promotional medical and scientific position. The MSL's key objective is to create impact through advancing clinical practice within the assigned territory that leads to improved patient outcomes. The MSL must demonstrate deep therapeutic expertise, understand territory and market influences, engage scientifically with Healthcare Providers (HCPs) and medical experts, manage, and develop their territory and execute all relevant activities in alignment with the medical strategic and tactical plan - while functioning within the Novartis Code of Conduct, Ethics/Compliance policies and Working Practice documents. The MSL will Inform and shape medical strategy through application of a curious mindset to collect impactful and actionable insights, understanding the potential strategic impact of critical insights.This territory will be responsible for covering Washington DC and the state of Virginia. The preferable location for the successful candidate to reside would be in the Washington, DC area.Role Responsibilities include, but are not limited to• The MSL will leverage scientific expertise and market knowledge to establish and build professional relationships and engage with HCPs (including community physicians, pharmacists, medical experts, nurses, and other healthcare professionals) and other thought leaders in geographical area as aligned with medical strategy • The primary responsibility of the MSL is to engage with customers - customer engagements may include but are not limited to: emerging data discussions, clinical trial activities, uncovering barriers in patient journey, understanding market dynamics within their territory, exploration of areas of unmet medical need, pipeline discussions, educating on disease state and product, capturing adverse events, and capturing medical insights through all stages of product lifecycle. • Must demonstrate strategic territory vision and ensure appropriate territory identification, mapping, and planning of Medical Engagements (MEs) and Key Accounts as aligned to medical strategy and in collaboration with internal Novartis colleagues. This includes:a. identification of key stakeholders with influence on the patient journey and in the disease space throughout theproduct development lifecycle to establish strategies for education, engagement, and partnershipb. identification of opportunities for partnership with academic centers, centers of excellence, and/or systems of care to drive impact within the assigned territoryc. identification of opportunities to involve HCPs or MEs wh

🧠🌍🚀 Medical Affairs professionals in neurology face significant challenges, and leveraging Real-World Evidence (RWE) can be instrumental in overcoming these hurdles. Let's delve into these pain points and explore how RWE can positively impact the field. 💪✨ 🔥 CHALLENGES: Medical Affairs professionals in neurology encounter unique difficulties, including: 1️⃣ LACK OF COMPREHENSIVE DATA: Limited access to real-world patient data often hampers their ability to understand disease progression, treatment outcomes, and patient experiences fully. 2️⃣ SLOW INNOVATION ADOPTION: Neurology lags behind in adopting innovative practices due to the complexity of the diseases, limited treatment options, and evolving landscape. 3️⃣ EVIDENCE GAPS: Traditional clinical trials may not capture the diverse patient population and real-world treatment outcomes, leaving gaps in evidence generation. 💡 RWE SOLUTIONS: Embracing RWE empowers Medical Affairs professionals in neurology to overcome these challenges effectively: 1️⃣ HOLISTIC PATIENT INSIGHTS: RWE provides vast, real-world patient data from multiple sources, enabling professionals to gain a comprehensive understanding of disease progression, treatment patterns, and patient experiences. 2️⃣ LEVERAGING TECHNOLOGY: By employing advanced analytics and AI-powered platforms, professionals can efficiently analyze complex neurology data, uncover patterns, and generate actionable insights to inform decision-making. 3️⃣ ACCELERATED INNOVATION: RWE facilitates the identification of unmet medical needs, aids in the design of more targeted clinical trials, and supports the development of personalized therapies, expediting innovation in neurology. 4️⃣ STRATEGIC COLLABORATIONS: RWE allows Medical Affairs professionals to collaborate with external stakeholders, including healthcare providers, payers, and regulators. This collaboration ensures that evidence generated aligns with the needs and expectations of all involved. RWE is key to bridging evidence gaps in neurology, enhancing treatment decision-making, and promoting patient-centric care. By leveraging this powerful tool, Medical Affairs professionals can drive better outcomes, accelerate innovation, and ultimately improve the lives of patients living with neurological disorders. Let's harness the potential of RWE to revolutionize neurology and pave the way for a brighter future! 🌟💙🧠 #MedicalAffairs #Neurology #RealWorldEvidence

Amidst corporate maneuvers, the Labcorp acquisition of Tufts Medicine's outreach lab extends diagnostic reach as a whole. This move prompts a reflection on the intricate balance between expansion and its broader impact, urging a blend of growth with ethical considerations. Looking ahead, Labcorp's deal with Tufts reflects healthcare's evolution in a market-driven world. These alliances are becoming the norm, streamlining services while disrupting employment. Balancing efficiency and empathy poses a challenge, requiring models that fuse growth with societal welfare. The future necessitates innovative approaches that prioritize community and individual well-being, not just financial gain. #Labcorp #Tufts #TuftsMedicine #Healthcare

#hiring *Clinical Trials Research Coordinator - Cancer/Brain Institute (Full Time, Day Shift)*, Miami, *United States*, fulltime #jobs #jobseekers #careers #Miamijobs #Floridajobs #HealthcareMedical *Apply*: https://lnkd.in/gSUhmBw2 Description Job Summary Coordinates clinical research studies on human subjects. Responsible for subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, report writing, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities. Responsible for new research application (including study start-up processes and requirements) and submission of protocols with subsequent amendments. Participates in protocol writing as needed and maintains initial and continuing education for Good Clinical Practice compliance. Job Specific Duties Attends and participates in investigator meetings, pre-study visits, and initiation meetings or coordinator meetings as appropriate. Collects and maintains accurate patient data for submission to Sponsor, maintaining proper patient records, coordinating the collection, and shipments of specimens as required by protocol. Communicates study objectives/procedures to relevant hospital units involved with the study including the establishment of good rapport with the Principal Investigator & providing required assistance. Communicates with the Sponsor or their representatives, schedules and facilitates study monitor visits, and facilitates communication between Principal Investigator and Sponsor or Sponsor s Representatives. Complies with the Research Finance Compliance policies and procedures including reporting requirements to research finance staff. Interacts with patients and families to recruit (screen, consent and enroll) study subjects and ensures compliance with the protocol. Responsible for speedy and adequate patient enrollment as determined by Research Management and Principal Investigator in all assigned studies. Submits new protocols to Research Regulatory Affairs team (for IRB submission/approval) and verifies proper document were received with the proper format. Submits amendments of protocols to Research Regulatory Affairs team and verifies the required corrections were inserted following the established procedures. Utilizes Good Clinical Practices in the conduct of clinical trials as per established protocol. Follows NCHS RI s Standard Operating Procedures, AAHRPP, HIPAA and FDA guidelines for clinical research, and keeps updated in those procedures and/or guidelines. Enters Research Patient information into CTMS within 72hours of enrollment, patient visit or patient-related event. Provides new Protocols, Amendments and study status updates to necessary research staff for digitization/entry into CTMS. Quali

#hiring Remote Physician Scientist, Clinical Development, Basking Ridge, United States, fulltime #jobs #jobseekers #careers #BaskingRidgejobs #NewJerseyjobs #HealthcareMedical #entrylevel #firstjob #newgrad #internship #entryleveljobs Apply: https://lnkd.in/dhk6JaAM Details Candidate can work 100% remote. This position is an 8 month contract with the possibility of extension or conversion to permanent. Pay for this position is 150.00 to 225.00 hourly depending on experience Job Description: Project - A mid-stage rare disease project in specialty medicine. In this position, you will become a critical member of the clinical development team to progress the rare disease project being developed for the treatment of a rare ectopic calcification disease PXE. In partnership with the global clinical leader, clinical operation lead, and in collaboration with external partners, you will serve as the Physician Scientist to lead the study team and the CRO operation team to successfully implement a project-critical Phase 2 trial. This critical path trial is designed to confirm the safety and tolerability and dose range finding in the target PXE population in preparation for a subsequent pivotal trial. Although straightforward in study design, the hybrid in-clinic-and-virtual trial conduct that integrates in-home nursing visit brings an exciting level of challenges and opportunities in this role. Specifically, you will work in close collaboration with the disease patient advocacy group and world-renowned PXE researchers. You will lead the client and CRO teams to execute the study activities, manage regulatory and ethics committee interaction, serve as the client medical monitor, expertly execute the study-end activities, and conduct data review and analysis. The major deliverables include but are not limited to strategic collaboration on study recruitment with the advocacy group, clinical trial investigator interactions, statistical analysis plan, study execution, medical monitoring, data analysis, and study reporting. Beyond the roles and responsibilities in individual clinical trials, you will assist the global clinical leader and contribute to the progression of this global project. The opportunities in the key roles include clinical development strategy, regulatory interaction, key investigator/leader engagement, collaboration with patient advocacy groups, establishment and management of Scientific Advisory Board and Safety Monitoring Committee, while working closely with key members of the project team members, and external subject matter experts. Skills: Drug Dev Experience: Three years or more of hand-on experience in leading clinical studies and clinical development programs as a demonstrated leader from clinical/clinical development department in pharmaceutical or biotech companies Common sense. Strong written and verbal communication skills Ability to