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The Digital Assistant Product Engineer will be responsible for developing innovative and interactive Digital Assistant products leveraging data, and advanced machine/deep learning, and recent advances in NLP and Generative AI. They will work with a matrixed team to design and scale Digital Assistant products such as Chatbots, Voice Assistants, Call Center Virtual Agents, and Avatar Digital Humans.
Seeking a Digital Assistant Product Engineer to lead the development of innovative Digital Assistant products using NLP, AI, and machine learning technologies to revolutionize patient care. Responsibilities include solution architecture, project management, technical leadership, and collaboration with key stakeholders. Requires a Master's degree and 6+ years of experience in enterprise software solutions, with a focus on Conversational AI/GenAI solutions and AWS development. Strong NLP/NLU knowledge and experience with leading Conversational AI platforms are essential.
The Healthcare Access Specialist is responsible for optimizing market access and reimbursement of the company's products in the healthcare sector. They develop and implement strategies to meet the needs of patients, service providers, payers, and health authorities. Responsibilities include understanding the healthcare environment, coordinating work strategies, developing relationships with stakeholders, and ensuring compliance with regulations.
The Germany Country Compliance Lead oversees the implementation of Pfizer's compliance program, leads strategic initiatives to mitigate risks, and collaborates with local leaders to ensure effective risk management. They provide subject matter expertise in Anti-Bribery and Anti-Corruption, serve as the primary compliance advisor, and manage a team.
Lead the creation and dissemination of Health Economic and Outcome Research (HEOR) to optimize reimbursement and pricing for Pfizer products. Engage with stakeholders, customize HTA materials, and ensure compliance with legislation while collaborating across teams for effective market access strategies.
The Hospital Regulatory Affairs Specialist at Phytopharma manages and ensures the validity of regulatory documents required for hospital procurement processes. Key responsibilities include collaborating with healthcare teams, tracking necessary documents, ensuring compliance with BOH regulations, and supporting product commercialization through timely submissions. This role works closely with various partners to align on requirements and facilitate approvals, aiming for efficient regulatory processes within the organization.
Manage a portfolio of non-interventional studies and economic models to assess clinical and economic value of products. Collaborate with teams to improve strategies, design studies, and maintain effective working relationships. Ensure statistical/methodological expertise while innovating solutions to complex problems.
The GMQG International Coordinator at Pfizer provides operational and administrative support in project management and system management to the Global Medical Quality Governance team. Responsibilities include maintaining project planning tools, coordinating meetings, managing documentation, and supporting regional training processes to ensure quality oversight initiatives are executed efficiently.
The Clinical Supply Strategist is responsible for coordinating clinical supply operations in LATAM, ensuring the timely delivery of supplies for clinical trials. This role involves managing import/export logistics, regulatory compliance, vendor oversight, performance monitoring, and communication between stakeholders.
As an Innovative Operations Lead, you will develop cost-effective commercial product sourcing strategies for clinical development programs, manage operational aspects of supply chain projects, collaborate with various teams, select appropriate vendors, ensure continuity of product supply, and maintain compliance to an IOL training curriculum.
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