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The Project Specialist will provide project-level support to the Project Lead and team members during all phases of assigned projects. Responsibilities include ensuring tools are set up according to SOPs, reporting project metrics, analyzing issues, and managing financial data. The role involves collaboration and contributes to improving patient health through clinical development solutions.
The Senior Quality Assurance Auditor at Parexel is responsible for leading, planning, scheduling, performing, and reporting GxP audits across all phases of clinical research. This role involves collaborating cross-functionally and managing audits while ensuring compliance with regulations, mentoring staff, and contributing to the development of strategic audit plans.
As a Site Contract Leader, you will oversee the site contracting process for clinical trials, ensuring timely execution of contracts. Your responsibilities include monitoring contract performance, advising on budgets, leading a site contracts team, developing best practices, managing budget control, and maintaining communication with stakeholders to facilitate effective contract execution.
The Statistical Programmer II will support programming activities related to clinical study data analysis and reporting, develop SAS macros, and ensure compliance with regulatory documentation. The role includes training and mentoring team members and maintaining communication with various project stakeholders.
The Senior Statistical Programmer will lead statistical programming efforts on projects, ensure adherence to timelines, and deliver high-quality services, including producing and validating derived datasets and documentation. They will also train and mentor team members, ensure compliance with regulatory standards, and participate in process improvements and audits.
The Site Contract Associate negotiates clinical site agreements (CSA) with sponsors, supports project leads in discussing budgets and ensures timely delivery of CSA start-up deliverables. Responsibilities include gathering study information, communicating strategies and timelines, maintaining databases, addressing potential issues, and coordinating with local teams to assure quality work.
As a Procurement IT Category Manager at Parexel, responsible for maintaining strong vendor relationships and optimizing procurement processes. Required knowledge and experience in IT category management with a focus on hardware and telecom.
Support the Statistical Programming group in analyzing and reporting clinical trials. Responsibilities include producing datasets, statistical outputs, and data listings using SAS Software. Opportunity to learn about the pharmaceutical industry and clinical trial processes.
The Study Start-Up Manager is responsible for managing and conducting start-up activities in compliance with procedures, guidelines, and regulations. They collaborate with CRAs and local study teams to ensure timely milestone achievement. Key responsibilities include trial and site administration, regulatory and site start-up tasks, and budgeting and agreements with investigational sites.
The Contracts Specialist at Parexel is responsible for drafting and negotiating contracts, preparing project budgets, and facilitating client interactions. They must ensure quality client deliverables, adhere to strict deadlines, and collaborate with internal teams for contract review and approval. The role requires strong organizational, communication, and analytical skills. A Bachelor's Degree in Life Science, Business, Languages, or equivalent is required.
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