- Merck (Rahway, NJ)
- …responsibilities:** + At least 3 years of experience in Research & Development Pharmaceutical domain operations, with proven expertise managing application ... and challenges at the intersection of healthcare, information and technology. We offer project -based rotations to help with your professional development , and a… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …works under the direction of the Thoracic Oncology Principal Investigator(s), Regulatory Operations Manager , Clinical Research Manager and / or directly for the ... Trials Office to complete the regulatory requirements of the clinical research project . The RC coordinates aspects of protocol submissions, prepares and submits… more
- Bristol Myers Squibb (Indianapolis, IN)
- …and implements policies and procedures for CMO compliance, including development of applicable Quality Agreements, Quality Business Processes, Product Disposition, ... 5 years' experience in quality assurance and/or compliance roles in the pharmaceutical industry. + Hands-on experience with QA oversight of contract manufacturing… more
- Taiho Oncology (Princeton, NJ)
- …evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower ... maintenance, and close-out. The SA I helps with the coordination of project activities, including corresponding with internal and external team members globally,… more
- IQVIA (Atlanta, GA)
- …Account Systems within the assigned geography. + Develops quarterly sales plans with the manager to align with the POA. + Manages client relationships to build an ... Account Systems within the assigned geography. + Develops quarterly sales plans with the manager to align with the POA. + Manages client relationships to build an… more
- Takeda Pharmaceuticals (Boston, MA)
- …Clinical Lead to lead the Clinical Sub Team (CST) accountable for the development and execution of the CDP. + Provide program-level sponsor's operational oversight ... spend related to clinical program execution. Works closely with COMs, Global Program Manager (GPM), and Finance to ensure on a regular basis that budgets, enrolment,… more
- Medtronic (Los Angeles, CA)
- …with the other functions within the Market Access team to support the development of evidence that will improve the understanding of the treatment of diabetes ... both systematic and targeted literature searches that will be foundational to the development of value dossiers suitable for HTA submissions in Canada and Latin… more
- Medtronic (Tempe, AZ)
- …closely with Manufacturing Operations, Process/Test Engineering, and New Product Development to gather requirements, improve production efficiency, and support new ... of current manufacturing automation software, test data and analytics software development . The candidate must have strong problem solving and analytic skills… more
- Kelly Services (Cincinnati, OH)
- …1st shift **Compensation:** DOE **SUMMARY** Reporting directly to the Senior Manager , Total Quality, the Quality Assurance Senior Compliance Coordinator will provide ... and practices meet regulatory requirements in a food, cosmetic, and pharmaceutical environment. The QA Senior Compliance Coordinator will be working directly… more
- AbbVie (San Francisco, CA)
- …Aesthetics on LinkedIn. Job Description At AbbVie, one of the largest pharmaceutical companies in the world. Our iconic brands include Botox, CoolSculpting, ... on. As the Staff Engineer, you will report to the Software Engineering Manager and continuously collaborate with key stakeholders across the business to solve the… more