Site Educator

• Good knowledge of clinical research and Good clinical practice certification is a must

• Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research

• Assess site to be in line with GCP.

• Orient research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits

• Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records

• Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies

• Assist research site with coverage planning related to staffing and scheduling for research projects

• Degree in life sciences or educational equivalent and relevant work experience in a clinical environment or medical setting; or equivalent combination of education, training and experience

• Applicable certifications and licenses as required by the company, country, state, and/or other regulatory bodies

• Extensive experience as a Senior Clinical Research Associate

PHYSICAL REQUIREMENTS

• Use of telephone and face-to-face communication requiring accurate perception of speech

• Use of keyboard requiring repetitive motion of fingers

• Frequent mobilization around the facility