Conduct all types of visits – site qualifications, initiation, interim monitoring, site management and study close-out visits
Review study subject safety information and informed consent and conduct source document verification for compliance, patient safety, and veracity of data
Actively participate in study team and investigator meetings
Compile and ensure completeness of regulatory documents and ethical submission documentation and review study subject safety information and informed consent and study material (e.g. CRFs, manuals)
Qualification & Experience
Four-year college curriculum in life sciences, OR
Two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and one year experience with clinical research (e.g. study coordinator, CTA, etc.)
Ability to meet the travel requirements of the job