IQVIA

Site Educator – Clinical Research

Casablanca-Settat

46 680 – 49 800 $ par anCDD / ContratSur site3–5 ansLicence / Bac+3Anglais, Français, ArabeSanté / ParamédicalSanté

L’essentiel du poste

Résumé par Postule AI

IQVIA seeks an experienced Site Educator for a one-year contract (0.5 days/week) to support clinical research operations in Morocco. The role involves managing clinical trial data, ensuring regulatory compliance, coordinating with investigators and research subjects, and maintaining GCP standards. Requires a life sciences degree, extensive clinical research experience, GCP certification, and fluency in English, French, and Arabic.

Vos missions

  • Provide clinical research support to investigators and review study protocols, CRFs, and electronic data capture systems
  • Collect and submit regulatory and ethics documentation to FDA and other regulatory bodies
  • Orient research subjects to studies and maintain adherence to staff training requirements
  • Prepare for and attend study monitoring visits, audits, and regulatory inspections
  • Support site coverage planning and assess sites for GCP compliance

Profil recherché

  • You have extensive clinical research experience and hold GCP certification
  • You are fluent in English, French, and Arabic and based in or willing to work in Morocco
  • You have strong attention to detail and can manage complex regulatory documentation
  • You excel at coordinating with multiple stakeholders and maintaining compliance standards

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About the Role

IQVIA is seeking a Site Educator to support clinical research operations. You will perform clinical procedures to collect, record, report, and interpret patient data for clinical studies, ensuring compliance with protocols, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines. This is a one-year contract position at 0.5 days per week.

Main Responsibilities

  • Provide clinical research support to investigators, including reviewing study protocols, Case Report Forms (CRFs), study documents, and electronic data capture systems
  • Attend all relevant study meetings and site requirement review meetings
  • Collect and submit regulatory and ethics documentation as required by the FDA and other regulatory bodies
  • Orient research subjects to studies, explaining purpose, procedures, timelines, and protocol requirements
  • Prepare for and attend study monitoring visits, audits, and regulatory inspections
  • Assist in maintaining staff training records and adherence to investigator site training requirements
  • Support site coverage planning for staffing and scheduling of research projects
  • Assess sites for GCP compliance

Required Skills

  • In-depth knowledge of clinical trials, protocols, consent forms, and study schedules
  • Knowledge of medical terminology
  • Proficiency with MS Windows and Office applications (Access, Outlook, Excel, Word)
  • Excellent interpersonal and communication skills
  • Strong attention to detail and ability to maintain effective working relationships
  • Fluency in English, French, and Arabic (essential for Morocco-based role)

Education and Experience

You must have a degree in life sciences or equivalent, with relevant work experience in a clinical environment or medical setting. Extensive experience as a Senior Clinical Research Associate is required. Good Clinical Practice (GCP) certification is mandatory, along with any applicable certifications and licenses required by regulatory bodies.

Physical Requirements

  • Telephone and face-to-face communication with accurate speech perception
  • Keyboard use requiring repetitive finger motion
  • Frequent mobilization around the facility

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