59 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...

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 Role Summary The Associate Director, Global Scientific & Value Content-Healthcare Professional (AD, GSVC-HCP) Vaccines & Infectious Diseases, position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This mid-level, headquarters-based position involves engaging with key stakeholders and managing the development and implementation of GSVC content and plans. This position engages key stakeholders by proactively creating and adapting the Value & Implementation (V&I) Planning & Scientific Platform for GSVC Annual Product and Disease State Plans. This position develops and adapts GSVC plans for products and disease states in the Vaccine and Infectious Diseases area aligned with V&I Plans. This position engages key stakeholders and incorporates medical insights into GSVC Annual Product Plans. This includes leading the...

Merck Job Description Role Summary The Associate Director, Global Scientific & Value Content-Healthcare Professional (AD, GSVC-HCP) Vaccines & Infectious Diseases, position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This mid-level, headquarters-based position involves engaging with key stakeholders and managing the development and implementation of GSVC content and plans. This position engages key stakeholders by proactively creating and adapting the Value & Implementation (V&I) Planning & Scientific Platform for GSVC Annual Product and Disease State Plans. This position develops and adapts GSVC plans for products and disease states in the Vaccine and Infectious Diseases area aligned with V&I Plans. This position engages key stakeholders and incorporates medical insights into GSVC Annual Product Plans. This includes leading the...

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...

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...

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 Under the direction of senior leadership, the Executive Assistant provides comprehensive administrative and organizational support to leadership in Global Quality. This role includes managing complex calendars, coordinating meetings and events, and handling domestic and international travel arrangements. The Executive Assistant ensures meeting readiness, manages individual expense reporting, and supports special projects as needed. The position requires interaction with a diverse group of internal stakeholders across all levels and locations, as well as external partners and visitors, while maintaining professionalism and confidentiality at all times. RESPONSIBILITIES: Administrative Support Provide diversified administrative support to senior leaders and their teams, including word processing, phone coverage, filing, mailings, and document management. Organize and maintain confidential and time-sensitive materials and files. Calendar & Meeting Management...

CSL The Opportunity: The Associate Director, in collaboration with Sales, Corporate Accounts, Business Operations and Medical Affair insures that functional area strategies are aligned with the overall HAEGARDA and BERINERT brand strategies. You will be accountable for overall sales, market share and management of HAEGARDA and BERINERT. You will be responsible for definition and implementation of HAEGARDA and BERINERT marketing strategies. You will develop new business opportunities for HAEGARDA and BERINERT and ensures timely and effective implementation. You will liaises with Medical Therapeutic Area Leaders and other key senior cross-functional stakeholders to ensure that customer needs are efficiently translated into effective initiatives. The Associate Director is responsible for the overall performance standards and objectives for employees in their assigned group. The Associate Director must be able to work independently with minimum guidance from the Executive...

CSL CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Director, Global Clinical Scientist Lead ? The job is in our King of Prussia, PA Waltham, Maidenhead UK or Zurich Switzerland office. This is a hybrid position and is onsite three days a week. You will report to the Global Clinical Lead, Hematology. You will be a key leadership role in the Clinical Development group, supporting professional development of 8-10 clinical scientist direct reports including providing strategic and tactical scientific leadership and guidance for clinical development activities in projects as assigned. You will help to drive quality scientific and operational...

CSL Associate Director, Corporate & External Affairs, R&D Portfolio Position Purpose: The Associate Director, R&D Portfolio Corporate and External Affairs, will lead corporate and external affairs communication strategy for CSL's R&D portfolio pipeline. The successful candidate will be responsible for driving communications for key pipeline milestones and clinical trials. They will serve as a strategic partner on R&D policy. They will lead issues and crisis management related to pipeline. In addition, they will strengthen the company's reputation within the biotech ecosystem and US to enhance and protect CSL's reputation and policy position. Reporting Relationships: Reports to: Head of Corporate and External Affairs, R&D Direct reports to position: 1 Main Responsibilities and Accountabilities: Serve as primary business partner and strategic advisor to SVP, Portfolio Development, SVP, Global Regulatory Affairs &...

CSL CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Senior Director Search & Evaluation Late TA Lead, (Im)? The job is in our King of Prussia PA, Waltham MA or Zurich Switzerland Office. This is a hybrid position and is onsite three days a week. Position Description Summary The Senior Director of Search & Evaluation will lead strategic sourcing and evaluation of later-stage external clinical assets in Immunology areas. You will focus on opportunities from Phase 2 through marketed drugs, requiring deep clinical expertise, strong engagement with external Key Opinion Leaders (KOLs) and clinical investigators, and a keen understanding...

CSL The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. Manages a team of programmers supporting clinical trial and integrated analyses, annual reporting, regulatory responses, publications, HTA requests and other purposes as needed within one or more therapeutic areas. The individual will work closely with the Senior Director, Clinical and Statistical Programming to advance the internal programming environment and statistical programming processes. Works closely with Statisticians to ensure that deliverables provided by internal resources or outside providers (CROs; FSP providers) are accurate and aligned with CSL standards. Main Responsibilities Working with the Biometrics Programming Leadership team, assess upcoming activities and resulting resource needs and allocate projects to people to ensure high...

CSL Position Summary: The Associate Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. The individual will work closely with the Director, Statistical Programming to ensure all assigned Statistical Programming tasks are managed to completion. They will work closely with Statisticians to ensure that deliverables provided by internal resources or outside providers (CROs; FSP providers) are accurate and aligned with CSL standards. This individual may manage a Therapeutic Areas (TA) or programs within or across TAs working with the Statistics TA lead to ensure all work required in the TA is completed within the project timelines with high quality. Main Responsibilities and Accountabilities : Working with the Director, Programming to assess upcoming activities and resulting resource needs and ensure high quality,...