•Independently responsible for all activities of the clinical trial including clinical site selection, study initiation visits, training of on-site personnel, study close-out visits and trial monitoring with on-site audits of clinical data for accuracy and completeness, and clinical report preparation and presentation.
•Prepare study protocols investigator manuals, site specific instruction manuals and design case report forms for new and modified products. •Assist with the ...
:: If you meet the qualifications listed below and would like more information contact Kimberly at 815-756-1221. Attach resume when responding to this posting ::
The Staff Scientist will be responsible for the product development of high molecular weight water-soluble polymers for use in industrial process applications.
-PhD in chemistry, polymer science, materials science
-3+ years of experience in polymer synthesis - waterborne
-Experience with inverse emulsions is a big plus
:: If you meet the qualifications listed below and would like more information contact Crystal at 815-756-1221. Attach resume when responding to this posting ::
The manager will be responsible for ensuring lab facilities operate efficiently, accurately, and within established regulatory guidelines.
-4 year science degree
-5+ years of experience in a lab environment
-2+ years of experience with responsibility for a lab in a prior role
-Experience with microbiology and molecular ...
Jul 7 -
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