Senior Medical Manager Cell Therapy Kite
1 month ago
Job Description
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. We empower our leaders to step up, share ideas, listen, learn, and lead. We’re welcoming bright, diverse, and imaginative minds; we’re nurturing them to foster an environment of inclusion and growth where innovation is encouraged. We expect our people leaders to model that environment, and to focus on creating inclusion, developing talent, and enabling teams.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. Join Gilead and help create possible, together.
Job Description
Senior Medical Manager Cell Therapy Kite, Denmark and Norway
Kite - a Gilead company is hiring a Senior Medical Manager to cover Denmark and Norway. Kite’s focus is on cell therapy in lymphoma and leukemia. As a Senior Medical Manager, you have both field-based as well as office-based responsibilities. You will be key in leading Medical Affairs initiatives in the respective countries and provide medical support to cross-functional team in the affiliate within cell therapy. You will report to the Nordic TA lead.
With a strong biomedical background, you bring relevant medical knowledge to both customers and internal teams, and support the teams by answering medical questions. This role is characterized by strategic thinking, leading medical affairs activities of the TA, cross-functional collaboration, all for which communication skills and business acumen are indispensable. You are responsible for liaising with key opinion leaders and healthcare professionals in academic and clinical centers for scientific exchange and data generation to ensure appropriate use of and preparing the landscape for cell therapy. The role is responsible for ensuring that medical affairs activities comply with pharmaceutical regulations and laws and providing expertise on drug safety and medical topics. Provides medical expert advice to ensure accuracy of data to support existing products or new product launches. Develops medical product information and stays informed on scientific trends and competition.
Responsibilities (include but are not limited to): Dedicates a significant percentage of time (≥50%) to field activities, meetings, presentations, and congresses Is responsible for establishing and maintaining appropriate scientific interactions with TA experts/opinion leaders and drives discussions and projects with the aim to integrate Develops the local medical plan of action (POA) in line with global strategic planning and contributes to the local affiliate cross-functional POA. Develops and executes projects and tactics according to the national strategic plan Organizes and participates at medical advisory boards Scientific data in clinical decision making for the benefit of patients Identify and collaborate with local experts on local data generation activities and assist with pipeline activities and liaises with Clin Ops Supports the development of local clinical data through clinical trials, investigator sponsored research and local sponsored studies Scientific input in HTA (Health Technology Assessment) dossiers and payer negotiations Represent the company to various groups of experts, medical professional groups, scientific societies, regulatory, payer groups or patient organizations
Skills & Knowledge
High willingness for continuous training and personal development Team worker with high social skills Proven ability to support cross functional teams in a medical role showing business acumen Excellent verbal, written and interpersonal communication skills including active listening Strategic thinking and open mindset Ability to build and maintain sound relationships with external and internal stakeholders Ability of transferring complex scientific/medical data into understandable medical communication and education Knowledge and adherence to external and company-related regulations Excellent communication, presentation and negotiation skills are required along with the ability to provide clear and concise analysis of quantitative and qualitative concepts Knowledge in project management In-depth knowledge of the therapeutic area (lymphoma, leukemia or hematology in general), the national healthcare system, and the medical environment You are located in either Denmark or Norway Business fluency in English and Danish or Norwegian High willingness to travel in Denmark and Norway and sometime international
Professional Training Degree in Medicine, Pharmacy or Life Sciences is required (PhD is desirable).
Experience Relevant experience must include at least 3 years in pharmaceutical industry and/or relevant clinical/ scientific experience Experience within therapeutic area of interest is desirable Experience in preparing and delivering scientific presentations is required Professional, clinical or research experience in a scientific or related field is desirable (minimum of 2 years preferred)
Gilead Core Values INTEGRITY – Doing What’s Right INCLUSION – Encouraging Diversity TEAMWORK – Working Together EXCELLENCE – Being Your Best ACCOUNTABILITY – Taking Personal Responsibility
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 for assistance.
For more information about equal employment opportunity protections, please view the ‘Know Your Rights’ poster.
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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:
Conformément à la Loi « Informatique et Libertés » (06/01/78), nous vous informons du fait que les données personnelles renseignées pourront faire l'objet d'un traitement informatique par Gilead et pourront être transmises aux Organismes Sociaux. Par ailleurs, vous disposez d'un droit d'accès, de rectification et de suppression des données vous concernant. Vous pouvez exercer ce droit en contactant: FranceDataPrivacy@gilead.com
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