Medical Information - Manager

Medical Information - Manager United Kingdom - Uxbridge
Medical Affairs
Regular
Job DescriptionAt 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 DescriptionThe Medical Information Manager is an integral member of the Medical Information (MI) team who utilizes therapeutic and product knowledge of Gilead Cell Therapy products to optimize internal and external customer communications. You will report to the Associate Director of Medical Information.Job OverviewThis job is fulltime and 3 days per week in the office are required.Expectations of this role include, but not limited to, researching, and preparing responses for MI inquires, as well as interfacing with and supporting MI escalations from the Medical Information vendor/call centre:Serves as the subject matter expert for MI on Gilead Cell Therapy products and associated therapeutic area(s)Responds to unsolicited medical requests regarding Gilead Cell Therapy 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 resources.Uses 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.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 role.Contributes to development of MI strategy and represents MI cross functionally.ResponsibilitiesRespond to unsolicited requests for medical and scientific information regarding Gilead Cell Therapy 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 relevant internal partners who may include medical affairs, development, regulatory, global patient safety and operations, commercial, to manage global response topics and content.Prepares and approves data on file to support response documents and 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 oversee and/or evaluate external consultant writers.May support MI booths at scientific congress and answer scientific questions – travel may be required.Identify, report, and record adverse events and product complaints in a timely manner in accordance with SOP.Serve as department SME for one or more product(s) or TA.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.Lead patient engagement initiatives such as the development of patient response documentsParticipate in development or update of department policy guidelines and SOPs.Participate and support department audit and inspection readiness.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 Cell Thearpy’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.Demonstrates Gilead’s core values and Leadership CommitmentsHas 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 environmentAwareness of digital solutions for communicating with healthcare providers and patientsPrevious experience with problem-solving and project management preferredPreferably, 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 othersDemonstrates strategic thinking. Reviews metrics regularly, to identify data gaps and develops strategy for creation of relevant content, in collaboration with internal partnersDemonstrates success in developing and maintaining good working relationships with internal and external stakeholders.Strong knowledge of, or ability to learn quickly, the TA and Gilead Cell therapy’ products.Education and ExperienceAn advanced degree (PharmD, MD) is preferred.Experience in Medical Information is required.Experience in Cell Therapy / Oncology is preferred.Experience in the pharmaceutical industry is required.Experience of working with MI vendors preferred.For jobs in the United States:As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact
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poster.Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.For jobs in France:
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Job Requisition ID
R0040946
Full Time/Part Time
Full-Time
Job Level
Manager
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