69 jobs found in Mansfield, NJ

Merck Job Description Position Title Associate Principal Scientist Department Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious Disease Brief Description of Position The Regulatory Affairs Headquarters Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team. They will have excellent communication and collaboration skills and will work closely with a global liaison(s) to help develop and implement a global strategy for registration and/or maintenance of VID products. Responsibilities may encompass all aspects of planning and implementation of a global regulatory strategy and regulatory submissions including assisting in preparing submissions, protocol review, and conducting research on regulatory guidances or competitive intelligence. Primary activities include, but are not limited to: * Assists in regulatory agency communications and...

Merck Job Description Position Title Associate Principal Scientist Department Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious Disease Brief Description of Position The Regulatory Affairs Headquarters Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team. They will have excellent communication and collaboration skills and will work closely with a global liaison(s) to help develop and implement a global strategy for registration and/or maintenance of VID products. Responsibilities may encompass all aspects of planning and implementation of a global regulatory strategy and regulatory submissions including assisting in preparing submissions, protocol review, and conducting research on regulatory guidances or competitive intelligence. Primary activities include, but are not limited to: * Assists in regulatory agency communications and...

American Red Cross Please use Google Chrome or Mozilla Firefox when accessing Candidate Home. By joining the American Red Cross you will touch millions of lives every year and experience the greatness of the human spirit at its best. Are you ready to be part of the world's largest humanitarian network? Join us-Where your Career is a Force for Good! Job Description: WHY CHOOSE US? Joining The American Red Cross is like nothing else - it's as much something you feel as something you do. You become a vital part of the world's largest humanitarian network. Joining a team of welcoming individuals who are exceptional, yet unassuming. Diverse, yet uncompromising in unity. You grow your career within a movement that matters, where success is measured in people helped, communities made whole, and individuals equipped to never stop changing lives and situations for the better. When you choose to be a force for good, you'll have mentors who empower your growth along a...

American Red Cross Please use Google Chrome or Mozilla Firefox when accessing Candidate Home. By joining the American Red Cross you will touch millions of lives every year and experience the greatness of the human spirit at its best. Are you ready to be part of the world's largest humanitarian network? Join us-Where your Career is a Force for Good! Job Description: Joining The American Red Cross is like nothing else - it's as much something you feel as something you do. You become a vital part of the world's largest humanitarian network. Joining a team of welcoming individuals who are exceptional, yet unassuming. Diverse, yet uncompromising in unity. You grow your career within a movement that matters, where success is measured in people helped, communities made whole, and individuals equipped to never stop changing lives and situations for the better. When you choose to be a force for good, you'll have mentors who empower your growth along a purposeful career...

Aledade Join our team as an Account Manager where you'll be the strategic bridge between healthcare practices and Aledade, driving success in value-based care contracts while directly impacting practice performance and revenue outcomes. You'll collaborate closely with health systems to align priorities and initiatives, ensuring both partners achieve their performance goals while advancing the shared mission of improving patient care through innovative value-based care models. This dynamic role offers the opportunity to build meaningful relationships with healthcare leaders while playing a crucial part in transforming how practices deliver and measure success in patient care. This role supports our New Jersey health system partner with approximately 25% travel to practices located along the New Jersey/Philadelphia border. Please note: candidates need to be residing in New Jersey or Philadelphia, PA to be considered. Primary Duties Represent the Aledade/Practice...

Merck Job Description Position Title Associate Principal Scientist Department Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious Disease Brief Description of Position The Regulatory Affairs Headquarters Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team. They will have excellent communication and collaboration skills and will work closely with a global liaison(s) to help develop and implement a global strategy for registration and/or maintenance of VID products. Responsibilities may encompass all aspects of planning and implementation of a global regulatory strategy and regulatory submissions including assisting in preparing submissions, protocol review, and conducting research on regulatory guidances or competitive intelligence. Primary activities include, but are not limited to: * Assists in regulatory agency communications and...

Merck Job Description Role Summary The Specialist, Scientific Leader Contracting, Global Expert Management and Strategy (GEMS) Consulting and Medical Education, position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This position is responsible for the process and training oversight of the outsourced Global Support Team in support of GEMS Consulting and Medical Education programs. This position also manages the coordination of ad-hoc projects in support of data integrity and related tasks. The Specialist is responsible for running routine and ad-hoc reports and may also support a variety of short- and long-term department initiatives. Responsibilities and Primary Activities Collaborates and integrates with U.S. and Global Business, Legal, and Compliance teams to ensure alignment of the Scientific Leader (SL) contracting process with all applicable...

Merck Job Description The Executive Director has the primary responsibility for strategy, oversight, and delivery of end-to-end activities involving new or marketed drug(s) for oncology indications. The Executive Director leads the team responsible for the cross-functional delivery of critical milestones in an oncology asset's lifecycle, spanning discovery through reimbursement, integrating the scientific, commercial, and manufacturing aspects critical to delivering clinically beneficial medicines to the right patients. The key to success is bearing the primary responsibility for developing, aligning, executing, and communicating the overall asset strategy. Specifically, the Executive Director may be responsible for: Creation, alignment, execution, and adaptation of the asset strategy cross-functionally Lead the asset development team to maximize the asset's potential Identifying registrational opportunities for pre-clinical and early clinical candidates which...

Merck Job Description Position Title Associate Principal Scientist Department Global Regulatory Affairs and Clinical Safety - Vaccine & Infectious Disease Brief Description of Position The Regulatory Affairs Headquarters Associate Principal Scientist supports products in the Vaccine and Infectious Disease (VID) therapeutic area as part of a regulatory team. They will have excellent communication and collaboration skills and will work closely with a global liaison(s) to help develop and implement a global strategy for registration and/or maintenance of VID products. Responsibilities may encompass all aspects of planning and implementation of a global regulatory strategy and regulatory submissions including assisting in preparing submissions, protocol review, and conducting research on regulatory guidances or competitive intelligence. Primary activities include, but are not limited to: * Assists in regulatory agency communications and...

Merck Job Description Role Summary The Specialist, Scientific Leader Contracting, Global Expert Management and Strategy (GEMS) Consulting and Medical Education, position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This position is responsible for the process and training oversight of the outsourced Global Support Team in support of GEMS Consulting and Medical Education programs. This position also manages the coordination of ad-hoc projects in support of data integrity and related tasks. The Specialist is responsible for running routine and ad-hoc reports and may also support a variety of short- and long-term department initiatives. Responsibilities and Primary Activities Collaborates and integrates with U.S. and Global Business, Legal, and Compliance teams to ensure alignment of the Scientific Leader (SL) contracting process with all applicable...

Merck Job Description The Executive Director has the primary responsibility for strategy, oversight, and delivery of end-to-end activities involving new or marketed drug(s) for oncology indications. The Executive Director leads the team responsible for the cross-functional delivery of critical milestones in an oncology asset's lifecycle, spanning discovery through reimbursement, integrating the scientific, commercial, and manufacturing aspects critical to delivering clinically beneficial medicines to the right patients. The key to success is bearing the primary responsibility for developing, aligning, executing, and communicating the overall asset strategy. Specifically, the Executive Director may be responsible for: Creation, alignment, execution, and adaptation of the asset strategy cross-functionally Lead the asset development team to maximize the asset's potential Identifying registrational opportunities for pre-clinical and early clinical candidates which...

Merck Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Medical Writer, , the review of accurate, clear, and compliant clinical, regulatory, and/or publicfacing documents in support of the company portfolio. The Medical Writer: Acquires and applies knowledge and understanding of medical writing responsibilities, including design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy). Demonstrates growing competence and independence in preparing clinical regulatory (e.g., clinical...

Merck Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Medical Writer, , the review of accurate, clear, and compliant clinical, regulatory, and/or publicfacing documents in support of the company portfolio. The Medical Writer: Acquires and applies knowledge and understanding of medical writing responsibilities, including design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy). Demonstrates growing competence and independence in preparing clinical regulatory (e.g., clinical...

Merck Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Medical Writer, , the review of accurate, clear, and compliant clinical, regulatory, and/or publicfacing documents in support of the company portfolio. The Medical Writer: Acquires and applies knowledge and understanding of medical writing responsibilities, including design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy). Demonstrates growing competence and independence in preparing clinical regulatory (e.g., clinical...

Merck Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials. The Medical Writer, , the review of accurate, clear, and compliant clinical, regulatory, and/or publicfacing documents in support of the company portfolio. The Medical Writer: Acquires and applies knowledge and understanding of medical writing responsibilities, including design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy). Demonstrates growing competence and independence in preparing clinical regulatory (e.g., clinical...

PerkinElmer Responsibilities Location King of Prussia, PennsylvaniaUS Job ID REQ-056619 Job Description Summary: Primary responsibility will be to assure the definition, implementation and maintenance of the Site Quality Management System in coordination with the senior management team, PKI engaged Quality Manager's expectations, Global PKI Quality Management policies, national, and international standards. This position provides the execution of the Quality System and conducting all aspects of that Quality Management System (QMS). Create awareness and provide training and education to all employees on quality processes and programs. Job Responsibilities Define, Consolidate and Integrate Quality Management Systems. Accept ownership for the Quality Management System between our Customer, PerkinElmer, and Third Party Service Providers (TPSP) by defining it and provide support and leadership necessary to integrate all the key internal and external quality...

CSL This position plays a critical role in advancing CSL's end to end Supply Chain transformation and operational maturity. Each member of the Supply Chain Excellence team is responsible for delivering strategic initiatives, enabling continuous improvement, supporting governance and strategy execution, and generating meaningful insights across global performance metrics. Responsibilities Lead and execute Supply Chain transformation initiatives using structured project management, ensuring delivery against scope, timeline, and budget. Identify, manage, and escalate risks, dependencies, resource needs, and issues across all assigned initiatives. Develop and deliver change management plans, stakeholder engagement strategies, and communications that enable successful adoption of new processes and ways of working. Facilitate continuous improvement activities (e.g., kaizens, VSMs, RCAs) and apply Lean/CI methodologies to drive measurable operational improvements....

CSL The E2E Integrated Business Planning (IBP) Integration Lead is focused on tactical, operational, and process-oriented execution of the IBP process to ensure the End-to-End alignment of plans, improvements, process adherence, performance management, and scenario coordination for executive decision-making. This role ensures the IBP process remains on-track and moving toward resolution of E2E plan decisions and escalations. A key accountability will be owning the E2E inventory performance, planning, and improvement for all nodes from plasma/API and raw materials to finished product. A successful candidate will be knowledgeable in current and future trends in supply chain management, integrated business planning, biopharma industry, and business financials. They will know how to get things done through formal and informal channels in a matrix organization given culture, policies, and politics with a broad understanding of business and strategies while anticipating future...

CSL Job Title: ERP Platform & Applications - SAP Basis Lead Role Overview The SAP Basis Lead is responsible for the technical integrity, reliability, performance, and lifecycle management of the enterprise SAP ecosystem across cloud (RISE PCE, BTP) and other platforms. Operating within an Agile/SAFe delivery model, this role ensures that the SAP technical landscape supports business operations, transformation initiatives, and platform evolution. The SAP Basis Lead works closely with product leaders, architects, managed service providers (MSPs), cybersecurity teams, and business stakeholders to deliver a secure, stable, and scalable platform. Key Responsibilities Strategic & Technical Leadership Own the technical strategy and roadmap for SAP Basis services within the ERP Platform & Applications domain. Ensure enterprise alignment with SAP best practices, clean-core principles, and upgrade-safe designs. Integrate SAP Activate phases with...

CSL Position Purpose: The Executive Director, Supply Chain Excellence Lead heads the Global Supply Chain Strategy Office as a multidiscipline department and is accountable for the strategic direction, governance, and execution of transformation and operational excellence across CSL's endtoend Supply Chain. The role directly manages a department spanning PMO/Change Management, Continuous Improvement (LEAN), Strategy Governance, and Analytics, and indirectly influences multiple global Supply Chain subfunctions, regions, and sites. Operating at the highest levels of complexity and ambiguity, this leader designs and steers the global transformation roadmap, modernizes systems and processes, and elevates supply chain maturity while safeguarding business continuity. As a member of the SVP's Supply Chain Leadership Team, this role partners closely with and collaborates extensively across CSL, including Finance Business Partners, Digital/IT, Quality, regional/site leaders, and...