Senior Pipeline Medical Science Liaison; Cardiovascular Metabolic Disease - South Region - Genentech
New Orleans, LA 70112
About the Job
The PositionSenior Pipeline Medical Science Liaison; Cardiovascular Metabolic Disease - South RegionThe OpportunityThe Senior Therapeutic Area Medical Science Liaison (TA MSL) is a credible scientific partner responsible for providing clinical and health economic information related to disease states and the appropriate utilization of Genentech medicines (approved and pipeline).
This field-based position will engage with healthcare providers, population health decision makers, and patients within their region(s), to further patient outcomes aligned with the overarching objectives of Genentech.
In collaboration with their regional partners, TA MSLs are accountable for co-creating the local medical strategy and delivering for their customers.
In addition, TA MSLs may be responsible for covering multiple medicines, as well as engaging in broad scientific discussions about patient outcomes and total cost of care, resulting in rich customer insights shared with key stakeholders across the organization.Specifically for this opportunity:We seek candidates to work on our early stage assets and simultaneously support the success of the clinical trials programs.This Senior MSL field-based role will work across Investigators and Health Care Professionals (HCP) to accelerate the development and delivery of medicines (initial focus on Obesity, Diabetes and related Cardiovascular Outcomes Programs) to patients through effective medical customer engagement in the development and potentially marketed phase of the product life cycle.Senior MSL’s will establish relationships with key external stakeholders and collaborate with internal partners sharing insights to inform and shape the global and local medical strategy while contributing to building early internal capabilities to enhance the launch readiness in the US.Territory and Preferred statesSouth Region:Texas, Oklahoma, Arkansas, Louisiana, Mississippi, Alabama, Georgia, Florida, North Carolina, South CarolinaKey ResponsibilitiesEnsure end-to-end customer experience for TA specific customers in the regionDemonstrate deep scientific expertise in assigned molecules/products and therapeutic areas to exchange relevant information with thought leaders and healthcare decision makersBuild and leverage relationships with key external scientific and medical customers to understand evolving healthcare trendsHaving proficiency in topics beyond scientific exchange, such as value/cost of care discussions and AE managementContinuous learning within the therapeutic area, active participation in upskilling programs, and adherence to guidelines and procedures.Specifically for this opportunity:Identify and support recruitment of high-impact, high-performing clinical research sites for a Phase II and III programsDevelops and facilitates relationships and collaborative networks with external stakeholders ensuring Genentech/Roche is the preferred partnerEngages and educates Investigators and site staff to enable and expedite successful delivery of clinical development programsProvides real-time insights and ground level understanding of the disease area landscape to better inform strategiesContributes to the high performance and innovation of team/ function to optimize customer experienceSupport, collaborate and be accountable to Cross-functional partners in Global, US Medical Affairs and the Clinical Research Organization (CRO) responsible for trial supportHealth Care Professional engagement and Therapeutic Area Expert development in the Cardiovascular Metabolic (CVM) spaceGaining insights that can help further inform our Commercial Develop Program (CDP) and clinical trials to reflect the current landscape and treatments for the Therapeutic Area (TA)Partners with cross-functional colleagues to enhance launch readiness in the USWho you areRequired Qualifications & ExperienceAdvanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN, NP, PA etc.).
BSN with extensive field medical experience with a pharmaceutical companyMinimum of 5 years related work experience (clinical, managed care, or industry experience) Prior experience as a field medical science liaison Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use)Relevant therapeutic area knowledge, comprehensive understanding of product and safety profiles, and familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry.Preferred ExperienceRoutine and tangible experience in a field medical role working with CRO and clinical operations.Candidates with 2+ years experience and deep and demonstrated understanding of cardiovascular, renal metabolic diseasesEarly and late stage clinical trial experienceRecent US Brand launch experience 2 or more years’ clinical or health economic research experience (either in industry or in another, related setting)In-depth knowledge of Phase IV/post-marketing drug developmentApplicants that live within the preferred states listed aboveTravel RequirementsBusiness travel, by air or car, is required for regular external business meetings with customers and intermittent internal company meetings (up to 70% of time)This position requires significant use of a company-provided car to perform the essential duties and responsibilities of the role.
As a result, Genentech, Inc.
(Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business.The expected salary range for this position is $163,700 - $303,900. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.BenefitsRelocation benefits are not available for this job posting.A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love. Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us.
Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.Job SummaryJob number:
This field-based position will engage with healthcare providers, population health decision makers, and patients within their region(s), to further patient outcomes aligned with the overarching objectives of Genentech.
In collaboration with their regional partners, TA MSLs are accountable for co-creating the local medical strategy and delivering for their customers.
In addition, TA MSLs may be responsible for covering multiple medicines, as well as engaging in broad scientific discussions about patient outcomes and total cost of care, resulting in rich customer insights shared with key stakeholders across the organization.Specifically for this opportunity:We seek candidates to work on our early stage assets and simultaneously support the success of the clinical trials programs.This Senior MSL field-based role will work across Investigators and Health Care Professionals (HCP) to accelerate the development and delivery of medicines (initial focus on Obesity, Diabetes and related Cardiovascular Outcomes Programs) to patients through effective medical customer engagement in the development and potentially marketed phase of the product life cycle.Senior MSL’s will establish relationships with key external stakeholders and collaborate with internal partners sharing insights to inform and shape the global and local medical strategy while contributing to building early internal capabilities to enhance the launch readiness in the US.Territory and Preferred statesSouth Region:Texas, Oklahoma, Arkansas, Louisiana, Mississippi, Alabama, Georgia, Florida, North Carolina, South CarolinaKey ResponsibilitiesEnsure end-to-end customer experience for TA specific customers in the regionDemonstrate deep scientific expertise in assigned molecules/products and therapeutic areas to exchange relevant information with thought leaders and healthcare decision makersBuild and leverage relationships with key external scientific and medical customers to understand evolving healthcare trendsHaving proficiency in topics beyond scientific exchange, such as value/cost of care discussions and AE managementContinuous learning within the therapeutic area, active participation in upskilling programs, and adherence to guidelines and procedures.Specifically for this opportunity:Identify and support recruitment of high-impact, high-performing clinical research sites for a Phase II and III programsDevelops and facilitates relationships and collaborative networks with external stakeholders ensuring Genentech/Roche is the preferred partnerEngages and educates Investigators and site staff to enable and expedite successful delivery of clinical development programsProvides real-time insights and ground level understanding of the disease area landscape to better inform strategiesContributes to the high performance and innovation of team/ function to optimize customer experienceSupport, collaborate and be accountable to Cross-functional partners in Global, US Medical Affairs and the Clinical Research Organization (CRO) responsible for trial supportHealth Care Professional engagement and Therapeutic Area Expert development in the Cardiovascular Metabolic (CVM) spaceGaining insights that can help further inform our Commercial Develop Program (CDP) and clinical trials to reflect the current landscape and treatments for the Therapeutic Area (TA)Partners with cross-functional colleagues to enhance launch readiness in the USWho you areRequired Qualifications & ExperienceAdvanced Clinical/Science Degree (e.g., MD, PharmD, PhD, MSN, NP, PA etc.).
BSN with extensive field medical experience with a pharmaceutical companyMinimum of 5 years related work experience (clinical, managed care, or industry experience) Prior experience as a field medical science liaison Proficiency in GCP (Good Clinical Practice) and ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use)Relevant therapeutic area knowledge, comprehensive understanding of product and safety profiles, and familiarity with managed care, health economics, reimbursement, and legal and regulatory landscape in the pharmaceutical/biotechnology industry.Preferred ExperienceRoutine and tangible experience in a field medical role working with CRO and clinical operations.Candidates with 2+ years experience and deep and demonstrated understanding of cardiovascular, renal metabolic diseasesEarly and late stage clinical trial experienceRecent US Brand launch experience 2 or more years’ clinical or health economic research experience (either in industry or in another, related setting)In-depth knowledge of Phase IV/post-marketing drug developmentApplicants that live within the preferred states listed aboveTravel RequirementsBusiness travel, by air or car, is required for regular external business meetings with customers and intermittent internal company meetings (up to 70% of time)This position requires significant use of a company-provided car to perform the essential duties and responsibilities of the role.
As a result, Genentech, Inc.
(Company) from time to time will check your motor vehicle record for purposes of determining your eligibility for driving a Company vehicle or driving any vehicle on Company business.The expected salary range for this position is $163,700 - $303,900. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance. This position also qualifies for the benefits detailed at the link provided below.BenefitsRelocation benefits are not available for this job posting.A healthier future.
It’s what drives us to innovate.
To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come.
Creating a world where we all have more time with the people we love. Genentech is an equal opportunity employer, and we embrace the increasingly diverse world around us.
Genentech prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status and veteran status.Job SummaryJob number:
202409-1239
30Date posted : 2024-10-31Profession: Medical & Government AffairsEmployment type: Full time
Source : Genentech