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;

DNS"

LI-DNI"

• Education : Bachelor’s Degree in Biology, Biological Sciences, or in a related field of study (will accept equivalent foreign degree);
• Training : None;
• Experience : One 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 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