Site Educator

About the Position

IQVIA is seeking a Site Educator for a contract position in Morocco. This role involves providing clinical research support, ensuring adherence to Good Clinical Practice (GCP), and assisting with study monitoring.

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, or 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.

Requirements

• 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.

We Offer

• Opportunity to work with a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry.
• Professional growth and development opportunities.
• Competitive compensation package.

About the Company

IQVIA is a human data science company™ that helps the entire biopharma industry come to new medical insights faster. We believe in the power of data to transform human health and anticipate a world where the right treatment is available for every person, every time.