Research Study Coordinator

Responsible for following established corporate policies and procedures to perform scientific investigative research and participate in carrying out research objectives; assist in the development of new methodologies and prepare material for incorporation into publications or for use in laboratory procedures; research literature in the field; conduct experiments and collect and analyze data using various degrees of statistical methodologies; collect biological samples from research models and utilize the samples in lab experiments; plan and set-up equipment for conducting experiments following established protocols and researching methodologies; gather data for analysis and interpretation of test results; gather and analyze data to assist in the development of abstracts and manuscripts for publication; utilize data gathered from lab work to perform measurements, interpretations and to report findings; work under the direction of Project Principal Investigators to develop materials for presentations including slides and posters; conduct critical analyses and evaluation of laboratory data generated on patients or from laboratory tests in order to formulate a hypothesis from the relationships found; plan and perform various types of experimentation; utilize data gathered from experiments to develop scientific protocols; process and record samples, order materials for assays, and determine schedules for assays planned; complete written progress reports and prepare summaries of data; prepare and maintain quality control records on assays ran in laboratory; utilize and apply knowledge of IRB compliance requirements, electronic data capture systems, research protocol development/implementation procedures, GCP guidelines, clinical trial enrollment activities, testing assessments, clinical data interpretation, and adverse events/response oversight to perform duties; monitor and maintain equipment and keep maintenance records on equipment for laboratory accreditation; keep abreast of new techniques and review literature in the field pertinent to the area of research; assist in writing papers for publication and scientific presentations based on research performed; develop research methodologies within the parameters of experimental protocols; research objectives to allow quantitative and qualitative evaluations and interpretation of data obtained; assist in the preparation of annual reports and in writing research proposals; and propose new ideas for discussion and advise on the feasibility of proposed research.

Location: Detroit, Michigan and multiple undetermined worksites throughout the US;

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Education: Bachelor's Degree in Biology, Biological Sciences, or in a related field of study (will accept equivalent foreign degree);

Training: None;

Experience: One (1) year in the position above, as a Clinical Research Associate, as a Clinical Research Assistant, as a Research Assistant/Research Associate, or in a related occupation;

Other Requirements: Must have one (1) year experience with all the following: IRB compliance requirements, electronic data capture systems, research protocol development/implementation procedures, GCP guidelines, clinical trial enrollment activities, testing assessments, clinical data interpretation, and adverse events/response oversight.

Will also accept any suitable combination of education, training and/or experience.

Additional Information

• Organization: Henry Ford Medical Group

• Department: Gastro Procedure - Main

• Shift: Day Job

• Union Code: Not Applicable