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Coordinate, develop, and execute client/sponsor contracts and change orders for projects. Assist legal and contracts group in preparing contracts and maximizing efficiency through administrative support. Maintain databases, track documents, create reports, and support process improvement initiatives.
The Project Manager will oversee and manage laboratory studies, ensuring client satisfaction and effective communication regarding study progress. Responsibilities include managing projects per regulations, attending client meetings, and training junior PMs. The role involves promoting process improvements and managing timelines and budgets for studies.
Seeking a Senior Contract Analyst to manage contractual agreements, ensure compliance, and contribute to the advancement of innovative treatments and therapies at ICON plc, a healthcare intelligence and clinical research organization. Responsibilities include reviewing and negotiating contracts, analyzing contract terms, providing guidance to project teams, maintaining contract records, and developing contract management processes. Requires Bachelor's degree in business or a related field, previous experience in contract administration, and strong analytical skills.
The Site Identification Lead is responsible for leading the site identification process for clinical studies, developing site identification plans and profile requirements, liaising with feasibility managers, and ensuring the integration of start-up plans with assigned project teams. They lead a team of specialists and manage the site identification budget to meet study delivery timelines.
As a Global Feasibility Manager, you'll lead clinical project feasibility processes to support proposal teams, assist in the generation of cost proposals, and provide strategic input to Business Development Operations, focusing on client interactions and partnerships.
As a Senior Auditor in Clinical QA at ICON, you will oversee internal audits, conduct quality assessments for clinical trials, report findings, and provide training to junior auditors while ensuring compliance with Quality Management Systems.
As a Global Feasibility Manager, you will lead the clinical project feasibility process, assist Business Development with cost proposals, and support strategic partnerships. You will be a technical expert in feasibility for clients and manage the delivery of awarded projects effectively.
Support the production team with quality assurance tasks, perform quality control checks on translated documents, ensure deliverables meet quality standards, liaison between production team and Quality team, and contribute to quality initiatives.
The Site Management Associate manages clinical studies by identifying, training, initiating, and closing study sites while ensuring compliance with protocols and timelines. Responsibilities include the preparation of regulatory documents and strategy development for site and patient enrollment, all under supervision according to local regulations.
The Senior Linguist will engage in language processing tasks and support clinical research activities. Responsibilities include ensuring quality in translations, collaborating with cross-functional teams, and contributing to language-related projects.
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