CLINICAL ASSOCIATE

Recognize, exemplify and adhere to ICON's values which center around our culture of accountability, integrity, partnership, collaboration and excellence in delivery.
• As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs • This is a developmental role which requires extensive training.
An ability and willingness to travel (drive and fly) as needed for this role and at least 60% of the time for future roles is required.
• *To acquire knowledge of ICH GCP, the conduct of clinical trials and governing regulations, relevant ICON SOPs, ICON internal tracking systems and client SOPs / client systems (when applicable) • *To assist the project teams with the set-up, organization and maintenance of clinical study documentation (e.
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Study Files, CRFs, etc.) and guidelines (as appropriate) including preparation for internal/external audits, final reconciliation and archival   • *To assist in the processing of Data Collection Forms i.
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log in, tracking, quality control as appropriate for the study   • *To share responsibility in the quality control audits of clinical study documentation (e.
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Study Files, CRF Files, Monitoring Files, etc.) to ensure study files are inspection ready at all times • *To facilitate and coordinate ordering/dispatching and tracking of trial materials (e.
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CRFs, diary cards, lab supplies, drug supplies, and study binders) as appropriate   • *To assist project teams with trial progress tracking by updating the Clinical Trial Management systems, providing access to study/client systems (as appropriate) • To run, review and analyze study reports for accuracy and work with the project teams to ensure updates are completed correctly • To assist in coordination of site/ study related payments, if applicable • *To contact and serve as a contact for clinical sites for basic requests (e.
., enrollment updates, missing documentation, meeting arrangements, etc.) • *To assist in the tracking and distribution of safety reports • To coordinate document translation, if required • To assist with, and attend the Project team meetings, and corresponding activities preparation, generation of meeting minutes and agendas • To assist in the production of slides, overheads, etc., as needed for project, departmental, sponsor and/or business development presentations • To assist with the coordination of various status and tracking reports including but not limited to team member tracking and training • To work in collaboration with internal and external colleagues to meet project objectives and timelines • To keep the Project Manager / Project Director / Clinical Operations Designee informed of any issues within the Project Team which require attention • To maintain client and patient confidentiality • Other duties as assigned Required.
• Bachelor’s degree or local equivalent, in life sciences or related discipline • Fluent English Level OFFICE BASED POSITION