Clinical Research Associate (CRA)

M42

  • أبو ظبي
  • دائم
  • دوام كامل
  • قبل 15 يوم
OverviewIROS is a leading Contract Research Organisation (CRO) in the Middle East, specializing in clinical trials across diverse therapeutic areas and integrating real-world data. We are seeking a highly qualified Clinical Research Associate (CRA) to join our team and play a key role in advancing clinical research excellence.About the RoleAs a Clinical Research Associate, you will be responsible for supporting clinical trial operations from study start-up through to close-out. You will collaborate with study sites, sponsors, and internal teams to ensure compliance, data integrity, and adherence to international standards of Good Clinical Practice (GCP).Responsibilities
  • Conduct feasibility studies and site qualification assessments.
  • Support study setup, including regulatory submissions and documentation.
  • Manage regulatory compliance and maintain essential study records.
  • Perform monitoring visits, review protocol deviations, and report adverse events.
  • Ensure data integrity and adherence to GCP.
  • Provide timely updates to clients and internal stakeholders.
  • Oversee study site closure and final documentation.
QualificationsEducation: Bachelor’s degree in Life Sciences.Experience: 4–6 years in clinical research, with direct involvement in at least five interventional clinical trials.Skills & Knowledge:
  • Strong organizational, decision-making, and time management skills.
  • Excellent communication and collaboration abilities, particularly in cross-cultural environments.
  • Proficiency in Microsoft Office applications.
  • Certification in Good Clinical Practice (GCP).
  • Demonstrated ability to lead, document thoroughly, and work effectively in a matrixed structure.

M42