Site Educator

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.

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