Performs informed consent procedures according to the ethical standards expressed in the Declaration of Helsinki, and facilitates screening processes in strict compliance with study protocols, standards of Good Clinical Practice, Standard Operating Procedures (SOP’s), QA/QC procedures, OSHA guidelines, Internal Review Board (IRB) approved Informed Consent Forms (ICFs) and other state and local regulations where applicable
Ensures the well-being and safety of participants complying with FDA and HIPPA regulations
Performs and/or participates in medical history collection/documentation, informed consent (ICF) and protocol reviews, assists with screening physicals and medical screening procedures
Prepares and maintains compliant study charts and documentation
Your experience and qualifications
A high school diploma or G.E.D.
A minimum of two years of experience in a research clinical environment is preferred
An equivalent combination of education and experience may be accepted as a satisfactory substitute for the specific education and experience listed above
Able to provide excellent customer service, with experience in public relations
Able to communicate professionally and effectively both verbally and in writing with participants from diverse backgrounds
Knowledge of medical terminology and procedures
Able to work independently and handle multiple competing priorities
Able to multi-task working within tight deadlines
Excellent organizational and time-management skills and a strong attention to detail
Proficient in MS Office Suite (Word, Excel, Outlook, PowerPoint)
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