Clinical Trial Assistant I Location: Madison, WI Duration: 6 Months with possible contract to hire Description: Summary: The main function of a clinical trials assistant is to assist the clinical research teams in ensuring the most effective and efficient conduct by providing administration and project tracking support. Job Responsibilities: To provide general administrative support to the Clinical Operations Department and assistance. To support the Clinical Operations teams with ongoing conduct of studies. To assist project teams with study specific documentation and guidelines as appropriate. Set up, organize and maintain clinical study documentation. Process Data Collection Forms i.e. log in, tracking, quality control as appropriate for the study. Assist in quality control audits of clinical study documentation. To assist in co-ordination of Investigator payments, if applicable. 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. Skills: Verbal and written communication skills, attention to detail, and problem solving skills. Basic ability to work independently and manage ones time. Basic knowledge of the information and techniques needed to diagnose and treat human injuries and diseases. Basic ability to analyze data and accurately document and record results. Education/Experience: High school diploma or GED required. Associate degree in medical technology or vocational training preferred. 0-2 years’ experience required. Day to Day Responsibilities of this Position and Description of Project/Assignment (What is a typical task breakdown & rhythm What level of interaction will this person have with the team? What will the work environment be like): Job descriptions are uploaded to req Assist w/research team Handle biological specimens Taking EKG/Vital Signs Looking for someone who might have a background in phlebotomy or specimen processing, Preferred but not required. Preferred Skills: Phlebotomy training Specimen processing As an equal opportunity employer, ICONMA provides an employment environment that supports and encourages the abilities of all persons without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.