Clinical research projects evaluate
the safety and effectiveness of drugs
and other medical treatments.
This requires attention to detail,
planning, and facilitation.
Clinical research coordinators
carefully organize clinical studies
to produce the most accurate results possible.
They maintain critical, legal records
of what goes on during studies,
including case reports and drug dispensation records.
Their data is essential in determining
the success or failure of a therapy.
These reports may need to be shared
with officials or other regulatory agencies.
Clinical research coordinators must exercise
clear ethical standards when it comes to screening,
monitoring, and directing study participants.
They ensure that participants understand
and voluntarily consent to a study.
Subjects may only participate in a study
after a clinical research coordinator interviews them,
reviews medical records, and consults with
the appropriate medical professionals
to ensure it is safe and responsible to do so.
They often advise sponsors of the study
on procedural issues and may schedule the facilities,
as well as analyze the risks of clinical studies.
Many clinical researchers work in research centers,
pharmaceutical labs, universities, and large hospitals.
Most work full time, and have a bachelor’s degree
with a major in a health sciences or related field.
Some employers require Coordinators
to have a Registered Nurse
or Licensed Practical Nurse
credentials for these positions.