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The Site Contracts Associate will negotiate Clinical Site Agreement templates with sponsors, support budget negotiations, manage CSA activities, and liaise with project leads to ensure timely deliverables. This role also involves coordination between various stakeholders and maintaining documentation for project success.
As a Project Specialist, you will provide project level support to the Project Lead and team members during all project phases. Responsibilities include setting up tools according to SOPs, reporting and analysis, and collating project financial metrics.
The Global Site Contracts Lead is responsible for negotiating Clinical Site Agreement templates, supporting project leaders in budget negotiations, managing CSA activities, coordinating between teams, and ensuring timelines and deliverables are met throughout the clinical trial process.
The Senior Technology Quality Auditor is responsible for leading and managing internal and supplier technology audits, ensuring compliance with regulatory standards. This role involves conducting audits, providing guidance on best practices, managing QA records, and fostering relationships with stakeholders. The auditor will support training and mentoring while maintaining knowledge of company policies and procedures.
The Senior Document Quality Reviewer is responsible for reviewing regulatory documents, performing quality checks, editing, and ensuring adherence to regulatory guidelines. This role involves coordinating with medical writers and consolidating feedback from other reviewers while leading quality control efforts and maintaining document consistency.
The Site Monitor II is responsible for ensuring compliance with regulatory, ICH GCP, and protocol at the site level. This includes monitoring data integrity and quality, conducting monitoring activities both remotely and on-site, verifying informed consent, and managing protocol deviations. Collaboration with the Site Manager and site staff to ensure the site's compliance and readiness for inspections is also essential.
As a Principal Biostatistician at Parexel, you will lead statistical analysis for clinical trials, ensuring project deadlines and quality are met. You will guide junior staff and help create impactful statistical plans and reports while collaborating with global teams to provide consistent high-quality services.
The Senior Analyst will develop and manage Oracle EBS Finance systems solutions, align finance-related applications with business goals, conduct requirements gathering, design documentation, support QA efforts, and help implement best engineering practices while mentoring junior team members.
The Oracle EBS Principal Analyst will manage and develop solutions for Oracle EBS Finance systems, address daily business issues, engage with various teams for requirement gathering, create documentation, support quality assurance efforts, and enhance internal processes.
The Senior Database Administrator will be responsible for managing Oracle EBS databases, ensuring production uptime, performance tuning, backup/recovery, and security. Key tasks include providing 24/7 support, collaborating with team members on technical standards, and consulting on SQL coding. The role requires leadership skills, strong analytical abilities, and effective communication with clients and IT management.
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