As clinical research associate I am responsible to onsite clinical trial study managment. Currently, I am concluding a phase of routine monitor visits and inititating database locks for 4 clincal trial studies at 17 sites.

Assist the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support. Recognize, exemplify and adhere to ICON’s values which center on our commitment to people, clients and performance. To provide a general administrative support to the Clinical Research Department and assistance to Project Manager(s) and Project Director (s). to assist the Clinical Research teams in completion of all required tasks to meet departmental and project goals. To be familiar with ICH GCP, appropriate regulations, relevant ICON SOP’s and ICON internal tracking systems. 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 project teams with trial progress tracking by updating the Clinical Trial Management Systems.