2 Marketing Applications Jobs

As a Senior Professional Campaign Developer, you will be responsible for the development, implementation, and execution of personalized marketing campaigns. Your ability to work on campaign optimizations, analysis, workflow, journeys, and act as a consultant for the tool technologies and marketing automation solutions will be crucial. You will be a Senior Campaign Developer with a proven track record in designing, developing, QA, and configuring Marketing Technology (AJO). Your advanced technical skills will be utilized to construct sophisticated ETL processes, enhance product functionality, and implement large-scale, real-time delivery of dynamic content communications. Demonstrating a comprehensive knowledge of multi-channel marketing strategies will empower you to lead insightful business discussions and engage directly with stakeholders on functional matters. Your role within the Marketing Platform team will be pivotal in driving client value through the implementation of marketing platforms for executing campaigns. You will focus on streamlining campaign launches, optimizing audience selection, and enhancing performance to deliver high-quality, targeted campaigns that meet client objectives and drive ROI. Your responsibilities will include campaign estimation, requirement gathering, solution design, platform setup with foundational schemas, performance monitoring, result analysis, and reporting. Additionally, you will think creatively to design and deliver complex solutions, enhance implementation and migration activities, offer technology consulting, stay current with new technologies, ensure precise documentation, and mentor team members to achieve client success and desired outcomes. Your responsibilities will include successfully leading and executing the design and development of marketing automation campaigns, implementing tracking and analytics solutions to measure the effectiveness of marketing campaigns and customer engagement, collaborating with marketing stakeholders to gather requirements and translate business needs into technical solutions, designing and implementing complex marketing campaigns via various digital channels, conducting code reviews, ensuring adherence to best practices and coding standards, configuring and optimizing dynamic content personalization, data manipulation, and integration with external systems, implementing audience segmentation strategies, developing custom reporting and dashboards, staying informed about industry trends, best practices, and emerging technologies, proactively identifying opportunities for process improvements, driving initiatives to increase operational efficiency and campaign effectiveness, mentoring junior developers, providing guidance on tool development best practices and methodologies, and troubleshooting and resolving technical issues related to tool configuration, data integration, and campaign execution. To qualify for this role, you should have a 4-year college degree in a technical field or equivalent and an Adobe campaign related certification. Additionally, you should have experience in technology integrations with Marketing technologies (AJO, ACC, AEP), a minimum of 1 year of experience with the AJO platform and more than 4 years working on Campaign implementations or manage projects, hands-on experience on the Adobe Campaign tool, 3+ years of SQL development experience, 3+ years of scripting/programming experience (JavaScript preferred), 1+ years of experience in cross-channel marketing campaign delivery, like Push Notifications, In-App deliveries, eagerness to learn new applications of traditional technologies, ability to articulate and convey technical concepts to a mixed audience, familiarity with enterprise software and project implementation life cycles, knowledge of CRM and/or marketing applications and processes, and knowledge of basic marketing concepts such as Campaign RoI metrics and KRAs.,

ABOUT THE ROLE Role Description: The International Regulatory Lead (IRL) Manager will provide regulatory leadership & expertise for International countries for one or more Amgen products. This role involves collaboration with various functions and local regulatory teams to optimize product development and regulatory approvals in International countries develop international regulatory strategy and provide regulatory support for in-country product registrations and life cycle management. Roles & Responsibilities: Advises Global teams on regulatory implications and requirements relevant to the global clinical development, Marketing Applications plans and objectives. Provides regulatory direction/expertise on the international regulatory mechanisms to optimize product development (e. g. expediting FIH studies, Orphan Drug, expedited regulatory designations, regulatory reliance mechanisms, compassionate use and pediatric plans). Under general supervision, plans regulatory submissions (e. g. clinical trial, marketing authorization applications and lifecycle management) for products within Amgens portfolio. Under general supervision, contributes to the development of international regulatory strategy documents (regulatory product filing plan, strategies, risks associated with the potential Agency outcomes and contingency planning, estimate likelihood of success) and communicates to others, as appropriate. Provides and maintains clinical trial and/or marketing application documentation (excluding Chemistry, Manufacturing & Controls documentation). May author documents/redact such documents to support a regulatory filing. Directs development of and manages the international label submission strategy, leads the negotiation activities with cross-functional teams and is accountable for the label deviation requests and outcomes. Supports local regulatory teams in triaging queries from health authorities, and where appropriate, helps identify existing responses to same or similar questions, leveraging knowledge management. Participates as a member of the Global Regulatory Team (GRT), and various global clinical and labelling focused teams. Shares regulatory information and implications with the GRT and other global teams on an ongoing basis and provides advice on international considerations. Partners with peers to agree on product strategy including projected submission and approval time. Maintains regular communications with the local teams to ensure alignment on strategy and to share product development status. Builds effective relationships and communication paths across the global, regional and local elements of the global regulatory affairs function. Maintains an awareness of new and developing legislation, regulatory policy and technical regulatory guidance relating to Amgen products. Performs regulatory research to obtain relevant histories, precedence and other information relevant to regional product advancement. Basic Qualifications and Experience: Doctorate degree OR Masters degree and 3 years of relevant regional regulatory experience OR Bachelors degree and 5 years of relevant regional regulatory experience OR Associate degree and 10 years of relevant regional regulatory experience OR High school diploma/GED and 12 years of relevant regional regulatory experience. Functional Skills: Must-Have Skills: Knowledge and experience in the international regulatory environment of clinical trial applications, non-clinical and/or clinical variations to marketing authorizations and product labelling relevant for biotechnology and/or oncology products Comprehensive knowledge of regulatory principles and understanding of regulatory activities, and how they impact other projects and/or processes General awareness of the registration procedures/challenges in International countries for Clinical Trial Applications, Marketing Applications and lifecycle management activities. Good-to-Have Skills: Ability to resolve conflicts and develop a course of action leading to a beneficial outcome Cultural awareness and sensitivity to achieve results across country, regional and international borders. Soft Skills: Strong communication skills, both oral and written Ability to understand and communicate scientific/clinical information Ability to work effectively with global, local and virtual teams High degree of initiative and self-motivation Planning and organizing abilities Ability to manage multiple priorities successfully Team-oriented, with a focus on achieving team goals Good negotiation and influencing skills. EQUAL OPPORTUNITY STATEMENT Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request an accommodation. .