IQVIA

Clinical Research Site Educator

Maroc

CDD / ContratSur siteLicence / Bac+3Anglais, Français, ArabeSanté / ParamédicalSanté

L’essentiel du poste

Résumé par Postule AI

IQVIA seeks an experienced Clinical Research Site Educator for a contract position in Morocco. This role involves supporting clinical trial operations by managing regulatory documentation, orienting research subjects, conducting site assessments, and ensuring GCP compliance. The ideal candidate has extensive Senior Clinical Research Associate experience, a life sciences degree, and fluency in English, French, and Arabic. This on-site position requires strong attention to detail, medical knowledge, and excellent communication skills.

Vos missions

  • Provide clinical research support to investigators by reviewing 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 explain procedures, timelines, and protocol requirements
  • Prepare for and attend study monitoring visits, audits, and regulatory inspections
  • Audit and maintain staff training records to ensure investigator site compliance
  • Assist with site coverage planning and staffing scheduling for research projects

Profil recherché

  • You have extensive clinical research experience and hold senior-level credentials
  • You are fluent in English, French, and Arabic and comfortable working in Morocco
  • You are detail-oriented with strong regulatory and compliance knowledge
  • You excel at communication and building relationships with diverse stakeholders
  • You are committed to maintaining GCP standards and ethical research practices

Généré automatiquement à partir de l’offre. Postule AI peut se tromper : vérifiez auprès de l’employeur.

About the Role

As a Site Educator at IQVIA, you will perform clinical procedures to collect, record, report, and interpret data on patients enrolled in clinical studies. You will support investigators in executing research studies according to protocols, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines, while assisting with daily workload planning.

Main Responsibilities

  • Provide clinical research support to investigators by reviewing study protocols, Case Report Forms (CRFs), study-specific documents, and electronic data capture systems
  • Attend all relevant study meetings and site requirement reviews to ensure compliance
  • Collect and submit regulatory and ethics documentation as required by the FDA and other regulatory bodies
  • Orient research subjects to studies, explaining purpose, procedures, and protocol timelines
  • Prepare for and attend study monitoring visits, audits, and regulatory inspections
  • Assist in maintaining staff training adherence by auditing and maintaining training records

Required Skills

  • In-depth knowledge of clinical trials, protocols, consent forms, and study schedules
  • Knowledge of medical terminology and GCP certification
  • Proficiency with MS Windows and Office applications (Access, Outlook, Excel, Word)
  • Excellent interpersonal and communication skills with strong attention to detail

Education and Experience

You should hold 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, along with applicable certifications and licenses as mandated by regulatory bodies.

Language Requirements

Fluency in English, French, and Arabic is essential for this Morocco-based position, as study documents are in English while French and Arabic are the local spoken languages.

Physical Requirements

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

Mise en forme par Postule ·

Signaler un problème