30 nurse jobs found in Collegeville, PA

GSK This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Provide strategic oversight of indirect reports who provide support for activities related to SDEA/PVASCs by: Ensuring that the direct reports provide the respective team support in consistently, efficiently and reliably delivering to regulatory requirements, third party commitments (implementation, maintenance and termination of SDE/PVASC) and organizational expectations and driving quality across the team. Ensuring the teams are staffed by appropriately skilled and trained individuals so that the team can successfully meet the required performance standards Developing and sharing pharmacovigilance and technical knowledge and experience with team members, with proven ability to support and coach direct reports Identify cases of potential noncompliance with internal and external procedures and follow appropriate procedures...

GSK Company Overview: At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people over the next 10 years. Our R&D division is dedicated to discovering and delivering transformational vaccines and medicines that prevent and change the course of disease. We are leveraging cutting-edge science and technology to build a deeper understanding of patients, human biology, and disease mechanisms, transforming medical discovery. We are revolutionizing the way we conduct R&D by uniting science, technology, and talent to get ahead of disease together. Job Description: As Principle Scientist PMed Operations specialising in Scientific Operations (SciOps), you will provide operational expertise to consistently implement the operational delivery of biomarker strategies developed by Clinical Biomarker and Virology leads within clinical trials, ensuring audit readiness at all times. You will be responsible for ensuring the appropriate...

GSK Would you like to be part of GSK's Global Epidemiology Department, with an opportunity to drive Epidemiology strategy and studies across the spectrum of drug development? If so, this is an excellent opportunity to explore. Our staff in Global Epidemiology provide leadership and expertise to develop and execute the Epidemiology strategy across the entire spectrum of drug development, from early drug discovery to registration and lifecycle management. As Director, Global Epidemiology, Hepatology, you will provide scientific leadership in the application of epidemiological expertise and methods to answer key challenges identified across all phases of medicine development for an asset or disease area to deliver new medicines more efficiently and effectively to patients. This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following: Develop, implement and drive evolution of GSK's short-,...

GSK Job Purpose: Ensure the development of appropriate regulatory strategies and their execution for assigned Vaccines asset(s) consistent with Medicines Development Strategy. This goal has to be achieved both as a component of an overall global regulatory approach and ensure compliance with both internal GSK process / policy and with regional regulatory requirements to deliver the best possible labeling, commensurate with the available data. Key Responsibilities: Accountable to GRL and Global Regulatory TA Head for development of appropriate regional and/or global regulatory strategies and for delivery according to plans. The Regulatory Director may be the single point of contact on assigned asset(s), responsible for regional and global regulatory strategies. In conducting role, planning will be on a multiple year horizon, with delivery requiring extensive matrix working within GSK to VP level and representing GSK with at least the local regulatory agency. Work closely...

GSK Director, Europe Regulatory Policy We seek a Director of Europe Regulatory Policy to join our Global Regulatory Policy & Intelligence team Job Purpose The Director, Europe Regulatory Policy will play a pivotal role in shaping regulatory policies and strategies in the Europe/EU region to ensure optimal advancement and life cycle management of GSK's biopharmaceutical portfolio. This role supports GSK's mission by driving advocacy and intelligence activities that influence the external regulatory environment for the benefit of patients and GSK. Key Responsibilities Develop and maintain Europe/EU regulatory policy, advocacy, and intelligence priorities to support and advance GSK's portfolio. Provide expert interpretation and advice on new legislation, guidelines, and regulatory policies, assessing their impact on GSK and our portfolio. Build and maintain strong relationships with external stakeholders, including regulatory agencies, industry trade...

GSK The Medical Director, Oncology Clinical Development will report to the Executive Medical Director, Clinical Development Lead (CDL), Oncology Clinical Development. The Medical Director will be responsible for clinical research activities pertaining to advancing the development of GSK's clinical portfolio and will also have responsibility for engaging in medical dialogues with relevant scientific and medical leaders in order to lead clinical data generation activities. This individual will also have a leading role in managing effective relationships with Key External Experts. This role requires a physician capable of developing and executing oncology clinical trials in support of the successful clinical development, regulatory filing and initial market launch of a growing portfolio of innovative and transformational Oncology agents. Collaborate with physicians, scientists, regulatory professionals, biostatisticians, regulatory, executive staff and others in a complex...

GSK Job Purpose Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets in clinical development and/or the post-marketing setting. Ensures scientifically sound review and interpretation of data and management of safety issues, escalating safety concerns to senior management and safety governance as appropriate. Makes recommendations for the further characterization, management, and communication of safety risks. Focuses on efficiency and effectiveness to meet the needs of patients and healthcare professionals globally. Supports pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure patient safety worldwide. If appointed as a manager (i.e., Team/Group Leader), is responsible for leadership of a team of individual contributors. Line management leadership competencies include resource and team management, coaching, influencing others, collaborative working, decision-making,...

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...

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. biotherapies used to treat serious and often rare conditions. Could you be our next Senior Manager, Total Rewards Management and Budget? This is a hybrid role located in our King of Prussia PA, Holly Springs NC, Summit NJ, Maidenhead or Liverpool UK, or Melbourne Australia office. You will report to the Associate Director of EMEA Benefits. CSL is seeking a highly skilled and experienced Senior Manager to lead our Total Rewards Vendor Management and Budget functions. In...

CSL Responsibilities: Associate Product Manager will help assist in the development and execution of tactics to advance brand strategy and achieve commercial objectives. This individual will support the Brand Director, and other members of the Brand Team, in creating and implementing key initiatives for HAEGARDA & BERINERT. The Associate Product Manager will measure and optimize the tactics they are responsible for. The ideal candidate will thrive in a fast-paced environment. This person should have confidence in regularly interacting with key stakeholders (Sales, Healthcare Systems, Medical, etc.) and be able to work collaboratively. Main Responsibilities: Assist in the logistical aspects of Peer-to-Peer programs, content development and KOL management in collaboration with medical affairs and medical education agency. Support the Marketing Team, working with training and field sales, to rollout new materials/initiatives for national business meeting, POA and ad-hoc...

CSL Lead the development of robust and data-driven forecasts for one of the three Franchises (Ig, Coagulation or Specialty) for the US market. Accountable for driving an objective view of demand and sales outlook for the business through robust analytics, data informed event sizing and epidemiological based forecasting where applicable, while incorporating inputs from market research, healthcare systems, Competitive Intelligence (CI) and other stakeholder insights. Strong communication and influencing skills with direct accountability for developing and implementing new forecasting platforms and ensuring accurate and timely forecasting deliverables and clear documentation of assumptions. Role requires strong consultancy orientation with ability to effectively and efficiently communicate to key brand stakeholders in the organization. Responsibilities: Manage all forecasting work streams for the franchise with a focus on model development and outputs Inform the analytical...

CSL The Opportunity Reporting to the Associate Director, Testing Center of Excellence and I&T Tools, you will lead the vision, delivery, and continuous improvement of Agile lifecycle capabilities across the enterprise. This role is pivotal in ensuring seamless integration of agile planning, collaboration, documentation, and quality assurance processes aligned with enterprise goals and regulatory standards. You will own and evolve a portfolio of tools-including Jira, Confluence, X-Ray, codeBeamer , and other Atlassian apps-ensuring they are optimized to support agile delivery, development, test automation, and compliance throughout the software development lifecycle (SDLC). You will also drive agile SDLC governance, including oversight of managed service partners that support the platform. This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid The Role Key Responsibilities: Product Ownership & Strategy: Define...

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 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...

Merck Job Description Position Description: The Vice President, Regulatory Affairs, General Medicine, will contribute to the mission and vision of the Global Regulatory Affairs and Clinical Safety (GRACS) function of Our Company's Research Laboratories (Research & Development) by: Developing an active engagement strategy with US FDA and global health authorities to advocate advanced regulatory strategies for novel medicines. Contributing to the continuous improvement of the operating model for regulatory activities in the US and globally to execute efficiently on regulatory obligations, compliance requirements and company strategy. Providing quality advice to stakeholders creating optimal development, commercialization, and drug/delivery device supply strategies Building our leadership and functional capability to keep pace with the changing science and regulatory environment. Establishing and effective implementation and oversight model to maintain...

Merck Job Description Position Description: The Vice President, Regulatory Affairs, General Medicine, will contribute to the mission and vision of the Global Regulatory Affairs and Clinical Safety (GRACS) function of Our Company's Research Laboratories (Research & Development) by: Developing an active engagement strategy with US FDA and global health authorities to advocate advanced regulatory strategies for novel medicines. Contributing to the continuous improvement of the operating model for regulatory activities in the US and globally to execute efficiently on regulatory obligations, compliance requirements and company strategy. Providing quality advice to stakeholders creating optimal development, commercialization, and drug/delivery device supply strategies Building our leadership and functional capability to keep pace with the changing science and regulatory environment. Establishing and effective implementation and oversight model to maintain...

Planned Parenthood Federation of America Planned Parenthood is the nation's leading provider and advocate of high-quality, affordable sexual and reproductive health care for all people, as well as the nation's largest provider of sex education. With more than 600 health centers across the country, Planned Parenthood organizations serve all patients with care and compassion, with respect, and without judgment, striving to create equitable access to health care. Through health centers, programs in schools and communities, and online resources, Planned Parenthood is a trusted source of reliable education and information that allows people to make informed health decisions. We do all this because we care passionately about helping people lead healthier lives. Planned Parenthood Federation of America (PPFA) is a 501(c)(3) charitable organization that supports the independently incorporated Planned Parenthood affiliates operating health centers across the U.S. Planned...

Aledade The Clinical Documentation Integrity (CDI) Coder is responsible for conducting comprehensive reviews of medical records to ensure the accurate assignment of diagnostic and procedural codes in alignment with provider documentation. This role is critical to maintaining compliance with organizational policies, ICD-10-CM, CPT, and HCPCS guidelines, as well as CMS regulations. Key responsibilities include ensuring precision and efficiency in coding to support the organization's value-based care initiatives. The CDI Coder serves as production staff, tasked with meeting established productivity and accuracy benchmarks while upholding data integrity and coding compliance standards. Responsibilities: Conduct detailed reviews of medical records to accurately assign ICD-10-CM, CPT, and HCPCS codes ensuring compliance with coding guidelines and payer-specific regulations. Identify and report documentation deficiencies or discrepancies impacting coding accuracy. Collaborate...