PAREXEL International Corporation Logistics Jobs in Covington

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Job Description : Duties : Provide statistical support for clinical research questions on Phase I-III clinical trial data in an FDA 21 CFR Part 11 regulated environment. Analyze Statistical Analysis Plans (SAPs). Perform statistical programming using SAS. Perform quality control on process and technical activities related to derived dataset, table, listing, and figure programming in accordance wi...
Job Description : The Principal Biostatistician works independently on all level complexity clinical trial projects, often with major regulatory impact. The person will be recognized internally and externally as a statistical expert. The Principal will lead projects and drive timelines and deliverables within the team. Key Accountabilities: Provide broad statistical support, including trial des...
Job Description : Provide quality oversight to project team management throughout the project. Specifically responsible for standard and risk-based quality interventions including: review of key project documentation, consultation, CAPA support, audit and inspection support, and collection and reporting of project quality metrics. Key Accountabilities: • Implement the standard quality evaluatio...
Job Description : Resolve complex technical problems as part of second level technical support. Analyze non-standard problems, develop technical solutions to meet each problem. Perform user training, work with other IT teams to develop and implement solutions. Provide support to hardware, software or application development efforts. Work with IT Service Desk to analyze and develop solutions to on...
Job Description : Essential Function Provide technical expertise, resource and mentoring for the implementation, computerized systems validation (CSV) and ongoing support & maintenance activities related to systems used by PAREXEL staff in the provision of their services. Work to the appropriate corporate standards of quality and efficiency, SOPs/Guidelines, ICH-GCP and/or other international re...
Job Description : Essential Function Conduct and facilitate specific start-up activities such as site identification, feasibility, SRP collection, review and approval, perform ICF customization, IRB/EC and MoH/RA submissions, and/or negotiate Clinical Site Agreements (CSA) with a high accountability on quality and timelines. Key Accountabilities: Appropriately plan and meet site activations wi...
Job Description : • Deliver best value and high quality service. • Ability to fill Statistical Programming Coordinator role on projects. The Statistical Programming Coordinator will: • Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to. • Coordinate and lead a statistical programming team to successful completion of a study within given timelines a...
Job Description : Duties : Provide technical expertise, resource, and mentoring for software quality assurance and testing of software applications in a bio/pharma domain setting. Apply domain knowledge of clinical and translational research and understanding of research methodology. Conduct functional, high-level systems integration, performance and regression testing of in-house developed softw...
Job Description : Deliver best value and high quality service. Ability to provide Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to. Coordinate and lead a statistical programming team to successful completion of a study within given timelines and budget. Monitor project resourcing, project budgets, and identify changes in scope. Ensure quality c...
Job Description : The Statistical Programming Coordinator will: Deliver best value and high quality service. Ability to fill Statistical Programming Coordinator role on projects. Input into and negotiate statistical programming timelines. Ensure that timelines are adhered to. Coordinate and lead a statistical programming team to successful completion of a study within given timelines and budg...
Job Description : Essential Function Performs clinical monitoring and investigational site /relationship management for designated EPD led clinical trials in accordance with ICH GCP, applicable regulations and SOPs. Act as PAREXELs direct contact with sites and is responsible for conduct of both on-site visits and remote/off-site communication/site management. Responsible to assess and ensure th...
Job Description : The Senior Procurement Specialist, Supplier Contracts will hold extensive contract negation experience with a strong knowledge base in contractual legal component. Demonstrated experience and achievements with Procurement services in either the Medical, Pharmaceutical, or Healthcare industries a plus. This role is expected to develop strong business relationships with customers...
Job Description : The Product Owner is responsible for working with Product Management, Operations, Subject Matter Experts and one or more Scrum teams to create a backlog of prioritized user stories which identify new product features and enhancements. The Product Owner then guides and supports one or more cross-functional Scrum teams by owning the vision for a release, deciding the priority and ...
Job Description : Overview: Provide medical expertise especially on imaging-related projects where imaging is used to evaluate the safety or efficacy of an investigational drug or device. Work closely with clients to develop strategies for the use of imaging in clinical trials. Key Accountabilities: Provide scientific expertise to project teams conducting clinical trials that rely upon the res...
Job Description : Essential Function This role is within the eClinical Platform Solutions group and focuses on supporting the development of functional requirements specifications and delivering eClinical solutions for eCPS owned products and integration services. It has a number of key requirements that include working in partnership with global functional, engineering and operational groups as...
Job Description : The Director of Business Controls is responsible for developing a self-governance culture within Individual Business Units. This person will be responsible for helping the business develop and deploy a proactive control and risk framework that is in line with enterprise and finance strategies and ensures the business remains in compliance with internal and external guidelines an...
Job Description : As a member of the PAREXEL Consulting Strategic Compliance Services group, provides GMP and quality system consulting advice, conducts audits, conducts training, and manages GMP compliance related projects for clients world wide. Reports factual findings, interprets facts, provides expert opinions, and makes recommendations for steps to take to address reported findings. May wor...
Job Description : Essential Function This position’s overall responsibilities are to assist the Regulatory Consulting team both with identification and review of regulatory issues likely to impact Liquent’s product suite and with providing support to our clients in the form of presentations and workshops focusing on Liquent’s product suite. Liquent’s product suite includes regulatory information...
Job Description : The Senior Procurement Specialist is expected to develop strong business relationships with customers (internal and external, typically at a mid-management level. This person provides in-depth specialized procurement knowledge, detailed strategic analysis and maintains ongoing commercial relationships between PAREXEL and its key suppliers. The Senior Procurement Specialist will ...
Job Description : Duties : Provide statistical support for clinical research questions on Phase I-III clinical trial data in an FDA 21 CFR Part 11 regulated environment. Analyze Statistical Analysis Plans (SAPs). Perform statistical programming using SAS. Perform quality control on process and technical activities related to derived dataset, table, listing, and figure programming in accordance wi...

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