Sr Manager, Medical Information

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.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 fulfil their aspirations. Join Gilead and help create possible, together.Job OverviewResponds to unsolicited medical requests regarding Gilead products from HCPs, members of the public, and internal Gilead colleagues. Responses are provided in a timely manner using approved standard documents, up-to-date literature support and other resourcesUses scientific and MI expertise to drive strategic initiatives and empower Gilead partners, HCPs, patients and other requestors with globally aligned resources that enable timely, informed decisions and improved patient outcomes.Prepares local resources (affiliate MI specialist).Identifies, reports and records adverse events and product complaints in a timely manner in accordance with SOP.May be asked to provide medical review for promotional and/or medical materials, depending on geography or roleContributes to development of MI strategy and represents MI cross functionally.ResponsibilitiesRoutine responsibilities may include the following, depending on geography:Respond to unsolicited requests for medical and scientific information regarding Gilead products and documents in the request handling system (MiQ).Researches and collaborates with cross functional colleagues to provide response to complex requests.Create, update, and participate in review, quality check and may approve MI response documents in accordance with local laws and regulations.Collaborates with affiliate internal partners who may include medical affairs, development, regulatory, global patient safety and operations, commercial, to manage global response topics and content.Prepares and support use of local response documents for resolution of complex requests.Maintain document repository with regular/routine review of approved documents for new data from regulatory updates, scientific conferences, up-to-date literature searches, proactive literature surveillance, or newly published materials.Understand the needs and preferences of internal and external partners and customers.Review and provide analysis of MI databases for trends, customer insights and data gaps to guide content development and prepare customer interaction reports to share with internal stakeholders.May plan and support MI booths at scientific congress and answer scientific questions – travel may be required. Affiliate specialists may participate in global conference support. May attend relevant sessions to enhance TA knowledge.Create TA and product training materials and provide training to cross functional colleagues and vendors.Support departmental strategic initiatives to address major activities within affiliate (product launches, labelling updates, patient engagement etc.)Execute and drive global initiatives and actions in a timely way to advance the provision of MI to improve patient care.May participate in events from external MI organisations across the pharmaceutical industry.Identify, report and record adverse events and product complaints in a timely manner in accordance with SOP.Participate in global and regional MI activities and projects in line with global and regional strategic MI plans.Serve as department SME for one or more product(s) or TA.Local affiliate specialist may participate as medical reviewer for local approvals as required.Manage local QA processes including the evaluation of medical request reports to ensure documentation and consistency in responses.Collect, present and share MI customer interaction reports (global or affiliate), identify data gaps and develop strategy for creation of relevant content.Collaborate with global MI team affiliate stakeholders to align for global content planning and therapeutic area strategy.Lead patient engagement initiatives such as the development of patient response documents (if local laws allow in affiliate market)Participate in development or update of department policy guidelines and SOPs.Lead/co-lead and partner with other affiliate MI teams on global and local MI initiatives and team projects.May have direct line management responsibilities for one or more non-permanent colleague e.g. contractor or MI fellow, with responsibilities as defined in the management track.Serve as liaison for all TA and department specific training for new staff members, cross-functional colleagues and vendors, as required.Manage local distributor or MI vendor, including quality and compliance.Lead timely communication of trends, customer insights and data gaps with key stakeholders.Affiliate MI Department Lead Responsibilities (without direct reports)Overall performance of the department and reports.Departmental compliance to local and global policies/ procedures relevant to Med Info.Quality and compliance of all departmental activities.Department audit and inspection readiness.QA and oversight of department and vendor.Report and customer interaction generation.Executing the global and local MI strategy.Development and maintenance of departmental policies and procedures relevant to MI.Participates as a member of the affiliate Medical Affairs leadership team; and participates in cross-functional affiliate projects/initiatives.Oversight of third-party vendor.Contribution and leadership in local and global cross-functional projects.Allocation of departmental resources.Continual improvement of the department.Increasing department visibility.Maintaining departmental budget and metrics.Setting direction for the department.Participates as a member of the affiliate Medical Affairs leadership team; and participates in cross-functional affiliate projects/initiatives.Knowledge and SkillsExcellent written, verbal and interpersonal communication skills, and the ability to work well in multidisciplinary teams, across geographies.Ability to create and provide clear communication of scientific data for different audiences, including members of the public.Knowledge and understanding of Gilead's marketed and investigational products.Knowledge of applicable regulatory and legal requirements for the provision of MI in the pharmaceutical environment, with understanding of regional or country regulations related to the provision of MI services.Ability to provide analysis and evaluate clinical, biomedical and scientific data.Ability to develop and maintain good working relationships with departmental and cross-functional colleagues.Understanding of internal and external stakeholder needs and priorities.Serve as an advocate for MI affiliate or Global MI.Demonstrates Gilead's core values and Leadership Commitments.Has a strong attention to detail, excellent project management and problem-solving skills, and ability to think creatively.Good organizational and work planning skills and ability to manage multiple projects in a fast-paced environment.Awareness of digital solutions for communicating with healthcare providers and patients.Previous experience with problem-solving and project management preferred.Preferably, prior specialist in MI at local affiliate or global level with ability to draw on previous experience.Strong problem-solving and project management skills preferred and ability to manage multiple projects in a fast-paced environment for both self and others.Previous leadership experience preferred.Demonstrates strategic thinking. Reviews metrics regularly, to identify data gaps and develops strategy for creation of relevant content, in collaboration with internal partners.Demonstrates success in developing and maintaining good working relationships with internal and external stakeholders.Ability to lead trainings for departmental, cross-functional colleagues and vendors. Ensures inclusion of relevant MI colleagues in medical affairs activities and trainings.For those who have responsibility for the work of others: demonstrated ability to manage and lead staff members.Strong knowledge of, or ability to learn quickly, the TA and Gilead products.Strong knowledge and understanding of all applicable local regulatory and legal requirements for Medical Affairs activities such as the provision of MI services.Ability to actively build cross functional relationships.Strong knowledge and understanding of all applicable local regulatory and legal requirements for Medical Affairs activities such as the provision of MI services.Education and ExperiencePharmacy, Nursing or Medical/ Life Sciences degree/advanced degree or equivalent.Experience in MI preferred or comparable experience within a healthcare/clinical environment required.Experience in the pharmaceutical industry or a MI vendor required.Levelling GuidePrevious experience minimum 7 years preferred (may include advanced degree course)For Current Gilead Employees and ContractorsPlease apply via the Internal Career Opportunities portal in Workday.Gilead Sciences, Inc. is a biopharmaceutical company that has pursued and achieved breakthroughs in medicine for more than three decades, with the goal of creating a healthier world for all people. The company is committed to advancing innovative medicines to prevent and treat life-threatening diseases, including HIV, viral hepatitis and cancer. Gilead operates in more than 35 countries worldwide, with headquarters in Foster City, California.#J-*****-Ljbffr