Clinical Research Assistant 2

To provide assistance in support of clinical research studies; assist with implementation and coordination of studies; participate in recruitment of study participants; perform behavioral or diagnostic testing; assist with collection maintenance amp; reporting of clinical research data.

Minimum Education Required:

Bachelor's Level Degree or equivalent combination of education and experience with a Major in biological sciences, health sciences, or medical field. 0 years of relevant experience required. 2-4 years of relevant experience preferred.

Required Qualifications:

Bachelors Degree in biological sciences, health sciences, or medical field, or equivalent combination of education experience; experience in research capacity desired; knowledge or experience in a specialty may be desired; experience in phlebotomy may be desired; experience performing basic laboratory procedures to process biological specimens may be desired; computer skill required with knowledge of database software applications desired. Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post-offer process.

25% CRA II will perform recruitment activities to identify potential research participants who are eligible to participate in specified clinical research protocols; recruits and schedules participants for visits

75% CRA II consents and enrolls participants, performs study activities as outlined in the protocol, enters data into the study data base, cleans and inventories research equipment and supplies; collects, extracts, codes, enters and assist with analyzing clinical research data; scans research records; transfers research data, generates reports and reviews to ensure validity of data supports activities to ensure compliance with all Institutional Review Boards (IRB).

Function: Research and Scholarship

Sub Function: Clinical Research

Career Band: Individual Contributor Series: Technical

Career Level:T2

This is a PERMANENT PART-TIME position working 20-25 hours per week.

25% CRA II will perform recruitment activities to identify potential research participants who are eligible to participate in specified clinical research protocols; recruits and schedules participants for visits

75% CRA II consents and enrolls participants, performs study activities as outlined in the protocol, enters data into the study data base, cleans and inventories research equipment and supplies; collects, extracts, codes, enters and assist with analyzing clinical research data; scans research records; transfers research data, generates reports and reviews to ensure validity of data supports activities to ensure compliance with all Institutional Review Boards (IRB).