Site Educator

IQVIA is looking for a Site Educator. Perform a variety of clinical procedures to collect, record, report and interpret data on patients enrolled and/or seeking enrollment in clinical studies according to the protocol, standard operating procedures (SOPs), and Good Clinical Practice (GCP). Assist with daily workload planning. This is a contract position for a year, 0.5 day RESPONSIBILITIES • Provide clinical research support to investigators to prepare for and execute assigned research studies, including Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data • Attend all relevant study meetings and review meetings for Site Requirements • Good command of English / French/ Arabic is a must for Morocco as all study documents are in English but French& Arabic are the local spoken languages • 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

SKILLS • Knowledge of clinical trials: In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules • Knowledge of medical terminology • Skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word • Excellent interpersonal and communication skills • Ability to pay close attention to detail • Ability to establish and maintain effective working relationships with coworkers, managers and clients

EDUCATION AND EXPERIENCE • 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