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#hiring *Medical Science Liaison (MSL) Solid Tumor Oncology Washington, DC*, Washington, *United States*, fulltime #jobs #jobseekers #careers #Washingtonjobs #DistrictofColumbiajobs #HealthcareMedical *Apply*: https://lnkd.in/gv2ga2Up 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
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#hiring *MSL Field Director, Immunology - Rheumatology (Northeast)*, Philadelphia, *United States*, fulltime #jobs #jobseekers #careers #Philadelphiajobs #Pennsylvaniajobs #ExecutivePositions *Apply*: https://lnkd.in/grFYaSsG Job Description Purpose: The Field Director, MSL (FD) plans, directs, coordinates and supports the activities of the Medical Science Liaisons (MSLs) within a designated geographic region to achieve scientific and business objectives within a therapeutic area of U.S. Medical Affairs. This includes, but is not limited to, coaching and mentoring for a designated number of medical level professionals (MSLs) in a therapeutic region. The FD reports to a therapeutic Field Medical Lead and works cross-functionally within U.S. Medical Affairs to identify, develop, implement, and monitor MSL strategies and tactics. Duties include strategic planning, financial management, personnel management, performance management process, regional awareness and expertise, data analysis, generation of metrics, material management, professional development, training, support, and execution of organizational goals and objectives. Responsibilities: People Leadership and Development: Recruitment and retention of key talent for AbbVie. Builds an organization reflecting a diverse and inclusive workforce through identification of team capability gaps and independent strengths. Establishes a productive work environment by creating trust and respect within the group and establishes self as a business partner. Consistently model "One-AbbVie" and AbbVie Ways of Working Leadership behaviors. People Leadership and Development: Provide coaching, mentoring and guidance that is consistent and timely to MSLs regarding their individual performance and progress, including annual performance reviews, growth and succession planning, and real time field reports based upon regular field travel combined with data analysis. Addresses performance issues decisively and appropriately in accordance with AbbVie's guidelines and Performance Excellence process. People Leadership and Development: Ultimate responsibility for scientific knowledge of self/team and oversight of MSL territory plans. Maintains clinical knowledge of designated therapeutic area and broad market knowledge of the region, including current treatment strategies, current and pending competitors, new therapeutic developments, payor dynamics, and other market issues/trends as it pertains to specific medical business interests. Regional Execution of Field-Medical Strategy: Maintain deep understanding of therapeutic strategy and interpretation of analytics to inform and maximize MSL Core Capabilities. Accountable for the direction and execution of MSL's regional goals/objectives and territory plans. Evaluate appropriate tools and analytics to ensure optimal trial performance through investigator engagement and ex
https://www.jobsrmine.com/us/pennsylvania/philadelphia/msl-field-director-immunology-rheumatology-northeast/469045842
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#hiring *MSL Field Director, Immunology - Rheumatology (Northeast)*, Philadelphia, *United States*, fulltime #jobs #jobseekers #careers #Philadelphiajobs #Pennsylvaniajobs #ExecutivePositions *Apply*: https://lnkd.in/grFYaSsG Job Description Purpose: The Field Director, MSL (FD) plans, directs, coordinates and supports the activities of the Medical Science Liaisons (MSLs) within a designated geographic region to achieve scientific and business objectives within a therapeutic area of U.S. Medical Affairs. This includes, but is not limited to, coaching and mentoring for a designated number of medical level professionals (MSLs) in a therapeutic region. The FD reports to a therapeutic Field Medical Lead and works cross-functionally within U.S. Medical Affairs to identify, develop, implement, and monitor MSL strategies and tactics. Duties include strategic planning, financial management, personnel management, performance management process, regional awareness and expertise, data analysis, generation of metrics, material management, professional development, training, support, and execution of organizational goals and objectives. Responsibilities: People Leadership and Development: Recruitment and retention of key talent for AbbVie. Builds an organization reflecting a diverse and inclusive workforce through identification of team capability gaps and independent strengths. Establishes a productive work environment by creating trust and respect within the group and establishes self as a business partner. Consistently model "One-AbbVie" and AbbVie Ways of Working Leadership behaviors. People Leadership and Development: Provide coaching, mentoring and guidance that is consistent and timely to MSLs regarding their individual performance and progress, including annual performance reviews, growth and succession planning, and real time field reports based upon regular field travel combined with data analysis. Addresses performance issues decisively and appropriately in accordance with AbbVie's guidelines and Performance Excellence process. People Leadership and Development: Ultimate responsibility for scientific knowledge of self/team and oversight of MSL territory plans. Maintains clinical knowledge of designated therapeutic area and broad market knowledge of the region, including current treatment strategies, current and pending competitors, new therapeutic developments, payor dynamics, and other market issues/trends as it pertains to specific medical business interests. Regional Execution of Field-Medical Strategy: Maintain deep understanding of therapeutic strategy and interpretation of analytics to inform and maximize MSL Core Capabilities. Accountable for the direction and execution of MSL's regional goals/objectives and territory plans. Evaluate appropriate tools and analytics to ensure optimal trial performance through investigator engagement and ex
https://www.jobsrmine.com/us/pennsylvania/philadelphia/msl-field-director-immunology-rheumatology-northeast/469045842
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Clinical Trialist - Physicians: Exciting Opportunity for a Clinical Research Career at a Well-Established Center in the Indianapolis Area. Even though I have been a principal investigator for >35 years for 550 trials in the cardio-metabolic area (more planned this year), I am mystified that this career choice has been ignored by the medical community in general. This has been significantly hampered by being employed by one of the different hospital systems in town. As a private business: (Remember when physicians were independent and had their own practice!!) 1. One does not have a non-compete contract. 2. One gets to pick and choose the appropriate trials in which to participate. 3. One is not forced to see 20-30 patients a day to keep the bean counters happy. 4. One has access to the new medications that one hopes will have a positive impact for people’s lives. Here are a couple of examples which have been exciting for me: Regarding every new cholesterol lowering drug on the market, I have been in one or more of the trials prior to drug approval (230 lipid trials). Regarding the new obesity medications (the GLP-1 and GLP-1 combinations), I have been in 12 trials so far and will participate in several more new ones, still this year. So, if physician/independent medical group might want to get involved, I would love to discuss opportunities that would be available.
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#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
https://www.jobsrmine.com/us/florida/miami/clinical-trials-research-coordinator-cancerbrain-institute-full-time-day-shift/466347400
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#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
https://www.jobsrmine.com/us/district-of-columbia/washington/medical-science-liaison-msl-solid-tumor-oncology-washington-dc/459865944
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At 4am on February 8th 2004 I was jolted awake on the blue leather sofa of the Doctors mess by a surgical bleep. By 9am on February 9th, I stood fully suited in the glass offices of Sanofi-Synthelabo on my first day as Medical Advisor. This year marks the twentieth anniversary of my departure from the NHS to join industry. Here’s my thoughts on that… 𝟭. 𝗦𝘄𝗶𝘁𝗰𝗵𝗶𝗻𝗴 𝗴𝗲𝗮𝗿𝘀: Leaving the comforting chaos of the NHS behind was like stepping into a new world. Instead of a bleep, I had a desk. Instead of a patient list, I had a budget to manage. Acute patient care was forgotten as I sought to understand data, regulations, and launch strategies. It took a full 18 months to recalibrate. 𝟮. 𝗧𝗵𝗲 𝗺𝗮𝗷𝗼𝗿 𝗱𝗶𝗳𝗳𝗲𝗿𝗲𝗻𝗰𝗲: If I could explain to anyone the fundamental difference between clinical medicine and what medics do in industry, it’s that patient care is necessarily reactive (a patient brings you a problem, you do your best to solve it, and then repeat), but in pharma, it's about proactivity and playing a much longer game - navigating regulations, collaborating with teams and planning for the future. Medics that thrive in industry understand this - they go after the work. 𝟯. 𝗜𝗻𝗱𝘂𝘀𝘁𝗿𝘆 𝗥𝗼𝗹𝗹𝗲𝗿𝗰𝗼𝗮𝘀𝘁𝗲𝗿 𝟭: In twenty years, the pharmaceutical world has transformed before my eyes. From the primary care blockbusters of my early years in industry, to biologics and specialist medicines for rare diseases. This is all because of very smart human beings working really hard to solve near-impossible challenges, and businesses that can support them whilst they do this. 𝟰. 𝗜𝗻𝗱𝘂𝘀𝘁𝗿𝘆 𝗥𝗼𝗹𝗹𝗲𝗿𝗰𝗼𝗮𝘀𝘁𝗲𝗿 𝟮: The resilience of our industry is remarkable. Business models run risks that no other industry would tolerate in the name of improving patient health. In two decades, I’ve seen large pharma organisations nearly wiped-out by a string of failures in R&D, only to rise again like a phoenix from the flames, whilst tiny, unheard-of organisations grow to employ hundreds of thousands of people. 𝟱. 𝗧𝗵𝗲 “𝗱𝗮𝗿𝗸 𝘀𝗶𝗱𝗲”: In industry I’ve been lucky enough to work with some of the brightest, most motivated and most ethical professional people I’ve ever met. Together they have solved the most complex drug development challenges over the course of years or sometime decades, all in the name of bringing a new medicine into the world. Anyone who thinks that working in industry is in some way a lesser career to clinical medicine, or worse, is less ethical simply don’t understand how our industry works or what we do for a living. There are dozens more – but my points would be the same: the biopharma industry is a superb example of how private enterprise can contribute to a better world. Thank you for welcoming me in, and making me a small part of the story.
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🔬 **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
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#hiring *MSL Field Director, Immunology - Rheumatology (Northeast)*, Charlotte, *United States*, fulltime #jobs #jobseekers #careers #Charlottejobs #NorthCarolinajobs #ExecutivePositions *Apply*: https://lnkd.in/gYFyz_VA Job Description Purpose: The Field Director, MSL (FD) plans, directs, coordinates and supports the activities of the Medical Science Liaisons (MSLs) within a designated geographic region to achieve scientific and business objectives within a therapeutic area of U.S. Medical Affairs. This includes, but is not limited to, coaching and mentoring for a designated number of medical level professionals (MSLs) in a therapeutic region. The FD reports to a therapeutic Field Medical Lead and works cross-functionally within U.S. Medical Affairs to identify, develop, implement, and monitor MSL strategies and tactics. Duties include strategic planning, financial management, personnel management, performance management process, regional awareness and expertise, data analysis, generation of metrics, material management, professional development, training, support, and execution of organizational goals and objectives. Responsibilities: People Leadership and Development: Recruitment and retention of key talent for AbbVie. Builds an organization reflecting a diverse and inclusive workforce through identification of team capability gaps and independent strengths. Establishes a productive work environment by creating trust and respect within the group and establishes self as a business partner. Consistently model "One-AbbVie" and AbbVie Ways of Working Leadership behaviors. People Leadership and Development: Provide coaching, mentoring and guidance that is consistent and timely to MSLs regarding their individual performance and progress, including annual performance reviews, growth and succession planning, and real time field reports based upon regular field travel combined with data analysis. Addresses performance issues decisively and appropriately in accordance with AbbVie's guidelines and Performance Excellence process. People Leadership and Development: Ultimate responsibility for scientific knowledge of self/team and oversight of MSL territory plans. Maintains clinical knowledge of designated therapeutic area and broad market knowledge of the region, including current treatment strategies, current and pending competitors, new therapeutic developments, payor dynamics, and other market issues/trends as it pertains to specific medical business interests. Regional Execution of Field-Medical Strategy: Maintain deep understanding of therapeutic strategy and interpretation of analytics to inform and maximize MSL Core Capabilities. Accountable for the direction and execution of MSL's regional goals/objectives and territory plans. Evaluate appropriate tools and analytics to ensure optimal trial performance through investigator engagement and excellen
https://www.jobsrmine.com/us/north-carolina/charlotte/msl-field-director-immunology-rheumatology-northeast/469045843
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#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/gVG-ryQs 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
https://www.jobsrmine.com/us/florida/miami/clinical-trials-research-coordinator-cancerbrain-institute-full-time-day-shift/465641496
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