天津招聘

职位描述：
CTA for global Top 1 company

? Recognize, exemplify and adhere to ICON's values which centers around our commitment to People, Clients and Performance.
? 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.
? Travel (approximately 10%) domestic and/or international
? *To provide general administrative support to the Clinical Operations (CRA) and assistance to Project Manager(s) and Project Director(s).
? To assist the Clinical Operations (CRA) /Project Management teams in completion of all required tasks to meet departmental and project goals.
? To support the Clinical Operations (CRA) /Project Management teams with ongoing conduct of studies.
? *To be familiar with ICH GCP, appropriate regulations, relevant ICON SOP’s and ICON internal tracking systems.
? To be familiar with the roles of the Clinical Research Associates (CRA) including site visits, if appropriate.
? To assist project teams with study specific documentation and guidelines as appropriate.
? *To set up, organize and maintain clinical study documentation (e.g. Main Study Files, CRFs, etc.) including preparation for internal/external audits, final reconciliation and archival.
? *To process Data Collection Forms i.e. log in, tracking, quality control as appropriate for the study.
? *To assist in quality control audits of clinical study documentation (e.g. Main Study Files, CRF Files, Monitoring Files, etc.).
? *To co-ordinate ordering/dispatch and tracking of trial materials (e.g. CRFs, diary cards, lab supplies, drug supplies) as appropriate.
? *To assist project teams with trial progress tracking by updating the Clinical Trial Management systems.
? *To copy and route incoming correspondence, internal documentation, CRFs, etc., as appropriate.
? To assist in co-ordination of Investigator payments, if applicable.
? *To contact clinical sites for specific requests (e.g., enrollment updates, missing documentation, meeting arrangements, etc.).
? *To assist in the tracking and distribution of safety reports.
? To co-ordinate document translation, if required.
? To attend project team meetings and generate meeting minutes.
? To assist the Project Manager and project team with Investigator Meeting coordination, activities preparation and generate meeting minutes.
? 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 team member tracking.
? Other duties as assigned


Pls contact Louisa for more detailed: Apple.Tang@docsglobal.com 举报 分享

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.