- Merck & Co. (North Wales, PA)
- Job DescriptionThe Senior Statistical Programmer, Study Data Tabulation Model (SDTM), provides oversight and creation of the Study Data Tabulation Model (SDTM) ... to external vendors and partners, and keeping current with industry submission data standards.The incumbent will be responsible for continuous improvement of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of initiative and ability to work independently and in a cross-functional management team.High level of business awareness. Travel: Global travel is required ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... team and serves as ad hoc member to the Global Project Team for late stage projects. This position...content templates and leads technical teams in preparation of submission documents to include clinical trial applications/amendments (eg, IND,… more
- Merck & Co. (Rahway, NJ)
- …Research and Development (ARD)-at our company's Research Laboratories is seeking a senior scientist to work onsite with extensive experience in validation & ... all modalities from our Research & Development Division to our Manufacturing Division global network. -You will work closely with other analytical groups in ARD ,… more
- Merck & Co. (North Wales, PA)
- …marketing of medical drugs and vaccines for the benefit of patients and global human health. This position supports statistical programming activities for late stage ... Activities :Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and good… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the Global MSAT team based in Raritan, NJ.Role OverviewThis position is a senior technical role in the global MSAT organization. This individual will be ... Responsibilities Represent MSAT at joint technical and CMC committeesPartner closely with senior Janssen technical team to achieve global alignment on all… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Responsibilities Represent MSAT at joint technical and CMC committeesPartner closely with senior leadership to achieve global alignment on all technical Carvykti ... with end-to-end know-how to manage process platform changes/improvements in a global manufacturing network and change management process.Candidate must have… more
- GXO (Hagerstown, MD)
- …ensuring organizational policies and procedures are understood and followed. As the Senior Director, Supply Chain Operations, you will be responsible for daily ... a company incentive plan.What you'll do on a typical day: Oversee the management of all client distribution and supply chain operationsSupport organic growth of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …include but not limited to Group Heads in Clinical Development, Asset & Portfolio Management , Global Clinical Operations, BDM and DLT members. He/she will also ... QA, and other functions as Pharm Tech SC and biologics, Corporate Business Management )Partner and collaborate with global marketing, global medical affairs,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... to budget, timeline, achievement of defined milestones and overall project risk management . He/she will assess project issues and develop resolutions to meet smooth… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …communication between CRO / vendors / AROAdditional non-study related activities: Occasional senior management interactions at FIHC, WDC; Initiates contact w/KOL ... medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Galapagos Federal Systems, LLC (Colorado Springs, CO)
- …missions, including managing SharePoint databasesExtensive Experience in Requirements Management and guiding senior leader decision-making processesStrategic ... training methodologiesDevelop and Maintain Training Materials for effective requirements submission processesKnowledge Management Expert with hands-on experience… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …documentation management needs for US and other health authority submission activities. + Responsible for tracking Clinical Trial Application (CTA) submission ... This individual will be responsible for supporting document management of Clinical Trial Applications (CTA) and related...the tracking of Reference Safety Information (RSI) approvals by global health authorities, and tracking for Global … more
- Internal Revenue Service (Kansas City, MO)
- …evidence of progressively responsible leadership and supervisory experience indicative of senior executive level management capability and directly related to ... Treasury is a major and influential leader in today's global economy. We have over 100,000 employees across the...on the negotiated start date or as directed by management . Salary for Senior Executive Service jobs… more
- Sanofi Group (Waltham, MA)
- …and/or discuss them with senior management . + Work with upper management on the allocation of Global Immunology headcount to meet project objectives. + ... and serving as an interface between scientific staff and senior management . The candidate will have scientific,...in alignment with the strategies agreed upon by the senior Global Immunology leadership team and … more
- Lilly (Indianapolis, IN)
- …life better for people around the world. Purpose: The purpose of the Senior Director/Executive Director, Global Regulatory Affairs, Global Regulatory Lead ... competitive developmentprograms/plans. + Ensure strategic messaging and content of global regulatory submission documents. Provide regulatory direction in… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work ... to those who need them, improve the understanding and management of disease, and give back to our communities...part of the Lilly post-approval regulatory group to support global submissions and registrations. As the project leader, you… more
- Georgetown Univerisity (Washington, DC)
- …interested in intellectual inquiry and making a difference in the world. Requirements Senior Grants Manager - Center for Global Health Practice and Impact ... Operations, they have the following core functions: + Grant Management : Oversee the administrative aspects of awarded grants, including...and Work Mode Designation Serving as part of the global health portfolio team, the Senior Grants… more
- Merck (Columbus, OH)
- **Job Description** **Role Summary:** + The Global Senior Director Medical Affairs (GDMA), Oncology is responsible for driving execution of scientific & medical ... They are impactful members of Product Development Team and sub-teams and Global Human Health commercialization teams. They collaborate with Global Commercial,… more
- Danaher Corporation (Raleigh, NC)
- …will lead the Regulatory Affairs department and report to the Vice President of Global Quality and Regulatory Affairs. The Director of Global Regulatory Affairs ... strategies for drug development and commercialization ensuring compliance with global regulations and standards across multiple markets. You will collaborate… more
