Gilead Sciences, Inc.
Sr. Director, Global Medical Content Management & Strategy
Gilead Sciences, Inc., Lakewood, New Jersey, us, 08701
Sr. Director, Global Medical Content Management & Strategy At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
Is this the role you are looking for If so read on for more details, and make sure to apply today.Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfill their aspirations. Join Gilead and help create possible, together.Job Description Gilead Sciences, Inc., a leading biopharmaceutical company dedicated to creating a healthier world for over three decades, focuses on developing innovative medicines to combat life-threatening diseases such as HIV, viral hepatitis, and cancer. With operations spanning more than 35 countries, Gilead is headquartered in Foster City, California, and is committed to advancing medical breakthroughs to improve patient lives globally.We aim to be a trusted source of unbiased, personalized, evidence-based clinical decision support for Gilead’s medicines provided through seamless multi-channel experiences to improve patient outcome. We are seeking a qualified and experienced individual to lead the global medical content and strategy for Medical Affairs.Job Overview: In this new role, you will be responsible for developing and leading a new strategy and operating model for the Medical Affairs scientific content ecosystem at Gilead including the creation, approval, and disposition of non-promotional materials used in external communications with HCPs, Patients, Patient Advocacy Groups, and other Healthcare organizations. In this role, you will develop solutions to support the innovation and automation of content creation and reuse for omni-channel delivery by leveraging tools and technologies (i.e., generative AI, component authoring, etc), to scale these efforts. You will collaborate with Medical Affairs Technology and Medical Excellence personnel, Legal and Regulatory personnel and Medical Affairs colleagues to evolve our content oversight, management and CRM platforms to enable an efficient review and approval of materials, ensure the proper storage and fulfillment of materials, and track how our medical content is used externally. You will develop metrics to assess efficiency and effectiveness of the MA scientific content ecosystem and use these metrics for continuous improvement and innovation.This position will also provide oversight and lead the operational support for the Medical Review Committee (MRC) for non-promotional medical materials, ensuring compliance with regulatory standards. This includes creating and managing all applicable SOPs, working practices/instructions, training materials and ensure that all applicable MRC team members are trained accordingly.This position reports into the Global Head of Scientific Communications as part of the Global Medical Strategy & Operations organization in Medical Affairs.Key Responsibilities:
Develop and implement comprehensive strategies and the operating model for innovating and leading the end-to-end process for scalable scientific content that includes the creation, approval, and disposition of non-promotional materials used in external communications the healthcare, patient, and scientific communities.Identify or develop new solutions to support the automation of content creation and reuse for multi-channel delivery by leveraging generative AI, component authoring, and other technologies to scale these efforts.Oversee procedural documents (i.e., standard operating procedures [SOPs], Work practices). Collaborate with therapeutic area Medical Affairs teams, Medical Information, Regulatory, and Legal to ensure adherence to regulatory requirements, industry standards and compliance with organizational policies and procedural documents in all aspects of medical review activities.Identify opportunities for process improvement with the scientific content ecosystem, utilizing data-driven approaches and stakeholder feedback. This includes coordinating and collaborating with the Medical, Scientific Communications, Legal, Regulatory leadership on execution of core projects related to process improvements and system enhancements.Partner with Medical Governance, Legal, Regulatory, and Medical Affairs leadership to establish protocols for quality assurance and monitoring of all aspect of medical approval and fulfillment activities, conducting audits and evaluations to maintain high standards of accuracy and reliability.Guide and coordinate vendor activities, including oversight of MRC coordinators and other 3rd party resources to support the operating model.Develop and deliver training to ensure that all content owners and reviewers are trained properly on the MRC process and other processes or technologies to support the scientific content ecosystem.Responsible for the development metrics and KPIs to measure the efficiency, productivity, quality, and use of the medical content created by Medical Affairs. Present findings to senior management with recommendations for further improvements to meet established KPIs.Assist with budget planning, forecasting, and managing accruals. Analyze resource utilization, forecast future needs, and develop strategies to optimize resource allocation to maximize efficiency and productivity.Education and Experience:Bachelor's Degree required: Doctor of Pharmacy Degree (PharmD) or Scientific/Medical Degree preferred.10+ years of program management experience leading medium to large scale initiatives; experience working in Medical Review Committee Operations is preferred.10+ years of medical affairs operational experience or medical/scientific communications experience.Strong project management skills with proven ability to prioritize, conduct, and meet project deadlines. Mastery of specific Project Management methodologies a plus (e.g., Lean, Six Sigma, PMP certification, etc.).Experience with Veeva Vault MedComms and Veeva CRM and partnering with IT colleagues to implement system enhancements.Excellent verbal and written communication skills as well as strong interpersonal and tactful negotiation skills.Proven ability to exercise problem-solving and strategic thinking skills; and has foresight and judgment in making complex decisions.Experience developing Policies, Standard Operating Procedures (SOPs), Work Practice Documents, etc.30% Travel.
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Is this the role you are looking for If so read on for more details, and make sure to apply today.Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfill their aspirations. Join Gilead and help create possible, together.Job Description Gilead Sciences, Inc., a leading biopharmaceutical company dedicated to creating a healthier world for over three decades, focuses on developing innovative medicines to combat life-threatening diseases such as HIV, viral hepatitis, and cancer. With operations spanning more than 35 countries, Gilead is headquartered in Foster City, California, and is committed to advancing medical breakthroughs to improve patient lives globally.We aim to be a trusted source of unbiased, personalized, evidence-based clinical decision support for Gilead’s medicines provided through seamless multi-channel experiences to improve patient outcome. We are seeking a qualified and experienced individual to lead the global medical content and strategy for Medical Affairs.Job Overview: In this new role, you will be responsible for developing and leading a new strategy and operating model for the Medical Affairs scientific content ecosystem at Gilead including the creation, approval, and disposition of non-promotional materials used in external communications with HCPs, Patients, Patient Advocacy Groups, and other Healthcare organizations. In this role, you will develop solutions to support the innovation and automation of content creation and reuse for omni-channel delivery by leveraging tools and technologies (i.e., generative AI, component authoring, etc), to scale these efforts. You will collaborate with Medical Affairs Technology and Medical Excellence personnel, Legal and Regulatory personnel and Medical Affairs colleagues to evolve our content oversight, management and CRM platforms to enable an efficient review and approval of materials, ensure the proper storage and fulfillment of materials, and track how our medical content is used externally. You will develop metrics to assess efficiency and effectiveness of the MA scientific content ecosystem and use these metrics for continuous improvement and innovation.This position will also provide oversight and lead the operational support for the Medical Review Committee (MRC) for non-promotional medical materials, ensuring compliance with regulatory standards. This includes creating and managing all applicable SOPs, working practices/instructions, training materials and ensure that all applicable MRC team members are trained accordingly.This position reports into the Global Head of Scientific Communications as part of the Global Medical Strategy & Operations organization in Medical Affairs.Key Responsibilities:
Develop and implement comprehensive strategies and the operating model for innovating and leading the end-to-end process for scalable scientific content that includes the creation, approval, and disposition of non-promotional materials used in external communications the healthcare, patient, and scientific communities.Identify or develop new solutions to support the automation of content creation and reuse for multi-channel delivery by leveraging generative AI, component authoring, and other technologies to scale these efforts.Oversee procedural documents (i.e., standard operating procedures [SOPs], Work practices). Collaborate with therapeutic area Medical Affairs teams, Medical Information, Regulatory, and Legal to ensure adherence to regulatory requirements, industry standards and compliance with organizational policies and procedural documents in all aspects of medical review activities.Identify opportunities for process improvement with the scientific content ecosystem, utilizing data-driven approaches and stakeholder feedback. This includes coordinating and collaborating with the Medical, Scientific Communications, Legal, Regulatory leadership on execution of core projects related to process improvements and system enhancements.Partner with Medical Governance, Legal, Regulatory, and Medical Affairs leadership to establish protocols for quality assurance and monitoring of all aspect of medical approval and fulfillment activities, conducting audits and evaluations to maintain high standards of accuracy and reliability.Guide and coordinate vendor activities, including oversight of MRC coordinators and other 3rd party resources to support the operating model.Develop and deliver training to ensure that all content owners and reviewers are trained properly on the MRC process and other processes or technologies to support the scientific content ecosystem.Responsible for the development metrics and KPIs to measure the efficiency, productivity, quality, and use of the medical content created by Medical Affairs. Present findings to senior management with recommendations for further improvements to meet established KPIs.Assist with budget planning, forecasting, and managing accruals. Analyze resource utilization, forecast future needs, and develop strategies to optimize resource allocation to maximize efficiency and productivity.Education and Experience:Bachelor's Degree required: Doctor of Pharmacy Degree (PharmD) or Scientific/Medical Degree preferred.10+ years of program management experience leading medium to large scale initiatives; experience working in Medical Review Committee Operations is preferred.10+ years of medical affairs operational experience or medical/scientific communications experience.Strong project management skills with proven ability to prioritize, conduct, and meet project deadlines. Mastery of specific Project Management methodologies a plus (e.g., Lean, Six Sigma, PMP certification, etc.).Experience with Veeva Vault MedComms and Veeva CRM and partnering with IT colleagues to implement system enhancements.Excellent verbal and written communication skills as well as strong interpersonal and tactful negotiation skills.Proven ability to exercise problem-solving and strategic thinking skills; and has foresight and judgment in making complex decisions.Experience developing Policies, Standard Operating Procedures (SOPs), Work Practice Documents, etc.30% Travel.
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