Clinical Trial Assistant I - ICONMA, LLC
Madison, WI 53704
About the Job
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.
Education/Experience:
High school diploma or GED required.
EMT, Phlebotomy, CMA or CNA certification or experience preferred
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, gender, sexual orientation, gender identity or express, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws.
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.
Education/Experience:
High school diploma or GED required.
EMT, Phlebotomy, CMA or CNA certification or experience preferred
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, gender, sexual orientation, gender identity or express, ethnicity, national origin, age, disability status, political affiliation, genetics, marital status, protected veteran status, or any other characteristic protected by federal, state, or local laws.
Source : ICONMA, LLC
