71 nurse jobs found in King of Prussia, PA

CSL Responsibilities: Develops a deep knowledge of the function supported and builds positive relationships throughout the supported function. Additionally, educate business partners about processes, roles, and capabilities of I&T that can create value for the supported function Ensures business value realization and optimization, develops, and maintains technology roadmaps, business case development, financial awareness, managing expectations, and identifying opportunities where technology can add value. Proactively serves as a trusted advisor and is the primary I&T point of contact to business line executives and managers. Provides highly valued strategic consulting level support and guidance through key I&T initiatives. Communicate decisions, priorities and relevant project information regarding business unit requests, projects, and initiatives. Leads a team of business partners, project managers, business analysts, an application support team consisting of...

CSL The Opportunity Reporting to the Associate Director, Identity Access Management Lead, you will lead the strategic direction, operational excellence, and continuous improvement of the enterprise directory services ecosystem-including Active Directory (AD), Entra ID, DNS, DHCP, PKI, and related infrastructure. You will ensure the delivery of secure, scalable, and compliant directory services across both enterprise and manufacturing environments, enabling reliable, modern, and integrated identity foundations to support hybrid and multi-cloud deployments. This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid The Role Responsibilities: Strategy and roadmap : Responsible for developing the strategy and roadmap for directory services that minimizes technical debt, maintains low complexity, and remains future-proof and flexible to support both on-premises and hybrid estates, driving towards establishing a unified cloud...

CSL Study Manager (m/f/x) - Clinical Trial Supply R-252424 Fullltime / permanent Multiple locations and hybrid working options available Responsibilities and Accountabilities Contributes to manage the Clinical Trial Supply budget and enable good cost controlling. Review invoices to verify accounting and formal accuracy and follow up with external vendors in case of discrepancies Tracking invoices to ensure processing within the agreed upon timelines allocation of invoices and services according to the pre-defined clinical supply cost structure Generation and maintenance of cost tracking reports to ensure good cost monitoring and cost transparency. Maintenance of the CTS budget and forecast sheets with planned and actual costs as well as accruals provided by the CTS study teams and the Finance departments in MBG and KoP Development and maintenance of an efficient filing structure for invoices to support the CTS TA teams in regards to cost transparency and...

CSL The Sr. Manager, Pricing & Government Reporting will lead the Government price reporting processes including monthly/quarterly calculations of pricing to Veteran Administration (VA), Public Health Services (PHS), and Centers for Medicare and Medicaid Services (CMS). Responsible for reconciling, preparing, and analyzing federal and state disclosures of product prices in order to meet federal reporting requirements. Additional responsibilities include: supporting commercial operations core business processes; implementing strategies and recommendations for improving processes, efficiency and practices; help to identify and prioritize service improvement opportunities and advise operational impact and help plan for implementation; assist in the development, update and review of Standard Operating Procedures (SOPs) related to the disclosure of marketing and healthcare expenditures to comply with federal and state legislative requirements. Main Responsibilites: Manage...

CSL CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives. With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspired to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring, CSL Plasma, CSL Seqirus and CSL Vifor. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions Could you be our next Director State Government Affairs? The job is located in the King of Prussia PA or Waltham MA area. Will consider other...

CSL The Opportunity: Reporting to the Director, Learning Operations, as the Associate Director of Learning Technology & Design , you will play a pivotal role in shaping learning strategies and experiences for the organization. You will lead the design, implementation, and evaluation of innovative learning solutions that align with business objectives and learner needs. You will have expertise in instructional design, learning technologies, and data-driven measurement strategies, combined with strong leadership and project management skills. You will stay abreast of learning content best practices and emerging technologies to drive innovation in learning and development initiatives. You will collaborate closely with learning departments across CSL functions and manage strategic oversight and governance of the enterprise LMS/LXP system. This is a dynamic and impactful role, offering the opportunity to lead innovation in learning strategies and technology, and contribute to...

CSL The IP Searcher plays a crucial role in supporting the IP team and broader business through carrying out, managing and coordinating comprehensive patent and trademark searches, maintaining records and managing regular IP monitoring activities within the IP team. The IP Searcher must possess strong research skills, attention to detail, and a deep understanding of IP databases and search techniques, including sequence searching and chemical sub-structure searching. Additionally, the IP Searcher works independently to coordinate and instruct external counsel and external search organisations on behalf of CSL and the IP team. The role includes developing and evolving the search capabilities of the IP function and may also include mentoring and overseeing work by a trainee/junior searcher. You will report to the Head of IP Digital & Technologies (IP LT). Responsibilities and accountabilities In conjunction with attorneys, design, coordinate and/or conduct IP searches...

CSL Position Title (Business Title): Executive Director, Digital Core Delivery Business/Functional Unit: I&T The Executive Director, Digital Core Delivery is responsible for all aspects of the digital core. At CSL, the digital core is the technology foundation that supports all aspects of CSL's business including cloud computing, networking, voice, and hosting. This role plays a pivotal role in driving the modernization and innovation of CSL infrastructure ecosystem to provide flexible, scalable platforms that can streamline data flows and integrate seamlessly with cloud services and other technologies. Working closely with the technology office, they will set priorities and standards, drive development and implementation, and manage strategic partners to ensure the digital core meet CSL requirements as it relates to robustness, security, reliability, scalability, consistency, and cost effectiveness. The leader will manage a team of IT professionals and...

CSL The Opportunity: Reporting to the Lead Counsel, Global Clinical Legal, as the Counsel, Clinical Legal , you will collaborate with the Global Clinical Development, provide practical, timely, and high-quality legal support to CSL's Global Clinical Development function on a wide range of legal and regulatory issues. Act as the primary escalation and resolution point for all clinical contracting legal queries emanating from the Clinical Contracts Project Managers. This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid The Role: Draft, review, and negotiate all agreements as directed by the Lead Counsel, Global Clinical Development, that are not managed by Counsel, Clinical Vendors, or the Clinical Contracts Specialist Team (CCST). This includes bespoke agreements for key strategic arrangements involving high risk and complexity. Collaborate with the R&D/Strategy transactional legal team to support all clinical...

GSK Are you interested in a leadership opportunity to drive the implementation of effective Clinical Oncology strategies for a multi-national pharmaceutical company? If so, this role may be for you! As the Director Clinical Sciences, Oncology, you will be responsible for building up the current Oncology development team, including recruitment of clinical scientists, and developing and leading GSK medium and long-term oncology development strategies for GSK's oncology pipeline. You will work closely with the Global Oncology Research and Development and Medical Affairs to ensure that the oncology clinical team have the highest quality capabilities and expertise. You will also ensure the optimal launch of new products and appropriate optimal patient use of currently available GSK Medicines through leadership and collaboration. In this role you will: Ensure delivery of quality study strategy and design, understand the analysis and interpretation of data throughout...

GSK The Governance and Best Practices Lead in the Global Scientific Communications organization is responsible for developing and implementing best practices and ways of working across Scientific Communications deliverables, establishing and enforcing communication standards and governance policies, and aligning strategy and governance to overarching global medical objectives. This role involves ensuring that GSK's data dissemination initiatives adhere to company and industry-level standards and best practices in the delivery of impactful integrated medical communication plans (IMCPs). Key Responsibilities: Lead the design and execution of best practices and processes for Scientific Communications IMCP deliverables across therapeutic areas (TAs) to address unmet audience needs, ensuring alignment with GSK's scientific communications objectives. Ensure consistency and quality across all IMCP deliverables by establishing clear guidelines and processes in partnership...

GSK The Operations Lead, Global Scientific Communications, Medical Information and Content Approval is responsible for supporting the VP, Global Scientific Communications and VP, Global Medical Information & Content Approval (GMI&CA) with operationalizing strategy, driving efforts to increase efficiency through centralized activities, and leveraging partners within and outside the organization to deliver objectives across Medical Therapeutic Areas (TAs). This role will be responsible for leading various initiatives across both organizations, managing budgets, and organizing team activities and communications. Key Responsibilities: Collaborate closely with the Scientific Communications VP and GMI/CA VP to drive delivery of overarching scientific communications and GMI & CA strategies in line with Global Medical objectives. Provide operational support and strategic insights to ensure alignment with GSK's global medical plans, assisting in the preparation...

GSK Are you a pharmaceutical oncology clinical development leader keen to unite science, technology and talent to get ahead of disease together in a company with an emerging portfolio seeking to make transformative breakthroughs? If so, this VP level career opportunity at GSK is worth consideration. GSK Oncology: We are leading the way to re-imagine improved ways of engaging with people with cancer and their loved ones. We have an opportunity to take an authentically human approach in our work with patients and their entire care team. We're building an inclusive culture where the world's best talent can help transform medicine together. The Career Opportunity: The VP-Oncology Clinical Development, Lung and Head/Neck Cancers will report to the SVP, Head of Oncology Clinical Development. The VP will be accountable for the design and implementation of the clinical development strategy across a portfolio of early- and late-phase assets in focused on lung and head/neck...

GSK Job Purpose Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting. Ensures scientifically sound review and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process to senior management and safety governance as appropriate. Makes recommendations for the further characterization, management, and communication of safety risks. Focus on efficiency and effectiveness to meet the needs of our Patients and HCPs. Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally. If appointed as a manager (i.e., Team/Group Leader) is responsible for leadership of a team of individual contributors. Line Management (including functional matrix reports) leadership competencies include resource and team management,...

Merck Job Description The Director of Global Site Agreements, Quality, Metrics and Process Improvement, is responsible and accountable for the strategic direction of the regional/specialty agreement teams over which they have oversight in alignment with overarching Global Site Agreements' and GCTO strategies. The Director will closely liaise with the Head of Global Site Agreements to implement global site agreement processes that are robust, efficient, and comply with Corporate Policies. This position will play a pivotal role in enhancing operational efficiency, quality and effectiveness in managing global site agreements. This position requires a blend of strategic leadership, project management expertise, and a strong focus on technology advancements to drive process improvements, ensure compliance, and enhance collaboration across business units. The ideal candidate will be an experienced leader capable of managing teams, engaging in complex problem resolution,...

Merck Job Description The Director of Global Site Agreements, Quality, Metrics and Process Improvement, is responsible and accountable for the strategic direction of the regional/specialty agreement teams over which they have oversight in alignment with overarching Global Site Agreements' and GCTO strategies. The Director will closely liaise with the Head of Global Site Agreements to implement global site agreement processes that are robust, efficient, and comply with Corporate Policies. This position will play a pivotal role in enhancing operational efficiency, quality and effectiveness in managing global site agreements. This position requires a blend of strategic leadership, project management expertise, and a strong focus on technology advancements to drive process improvements, ensure compliance, and enhance collaboration across business units. The ideal candidate will be an experienced leader capable of managing teams, engaging in complex problem resolution,...

Merck Job Description Role Summary The Associate Director (AD), Medical Omnichannel, is a key position within Medical Modernization in the Value & Implementation (V&I) Medical Affairs team, reporting directly to the Global Director of Medical Omnichannel. This role is essential in assisting the Medical Affairs Omnichannel function to define and execute the Medical Omnichannel Strategy, Roadmap, and Orchestration Plan in a highly regulated medical space, while coordinating execution and pull through across regions and markets with key stakeholders. Responsibilities and Primary Activities Strategic Development: Collaborate with the Director of Medical Omnichannel and cross-functional teams to stand up new digital medical channels and drive the development and orchestration of owned and paid channels within Medical Affairs omnichannel capabilities. Data and Metrics: Assist in the evaluation and selection of data, tech, channels, metrics, and vendor...

Merck Job Description Role Summary The Associate Director (AD), Medical Omnichannel, is a key position within Medical Modernization in the Value & Implementation (V&I) Medical Affairs team, reporting directly to the Global Director of Medical Omnichannel. This role is essential in assisting the Medical Affairs Omnichannel function to define and execute the Medical Omnichannel Strategy, Roadmap, and Orchestration Plan in a highly regulated medical space, while coordinating execution and pull through across regions and markets with key stakeholders. Responsibilities and Primary Activities Strategic Development: Collaborate with the Director of Medical Omnichannel and cross-functional teams to stand up new digital medical channels and drive the development and orchestration of owned and paid channels within Medical Affairs omnichannel capabilities. Data and Metrics: Assist in the evaluation and selection of data, tech, channels, metrics, and vendor...

GSK The Operations Lead, Global Scientific Communications, Medical Information and Content Approval is responsible for supporting the VP, Global Scientific Communications and VP, Global Medical Information & Content Approval (GMI&CA) with operationalizing strategy, driving efforts to increase efficiency through centralized activities, and leveraging partners within and outside the organization to deliver objectives across Medical Therapeutic Areas (TAs). This role will be responsible for leading various initiatives across both organizations, managing budgets, and organizing team activities and communications. Key Responsibilities: Collaborate closely with the Scientific Communications VP and GMI/CA VP to drive delivery of overarching scientific communications and GMI & CA strategies in line with Global Medical objectives. Provide operational support and strategic insights to ensure alignment with GSK's global medical plans, assisting in the preparation...

GSK The Governance and Best Practices Lead in the Global Scientific Communications organization is responsible for developing and implementing best practices and ways of working across Scientific Communications deliverables, establishing and enforcing communication standards and governance policies, and aligning strategy and governance to overarching global medical objectives. This role involves ensuring that GSK's data dissemination initiatives adhere to company and industry-level standards and best practices in the delivery of impactful integrated medical communication plans (IMCPs). Key Responsibilities: Lead the design and execution of best practices and processes for Scientific Communications IMCP deliverables across therapeutic areas (TAs) to address unmet audience needs, ensuring alignment with GSK's scientific communications objectives. Ensure consistency and quality across all IMCP deliverables by establishing clear guidelines and processes in partnership...