Healthcare and MedicalFull-TimeEntry-level(0-1 yr)
Job Description
Role Overview
IQVIA is seeking a Compliance Clinical Trials Assistant to support compliance activities within clinical trials. This role ensures regulatory standards, standard operating procedures (SOPs), and Good Clinical Practice (GCP) guidelines are maintained throughout the clinical trial process.
Key Responsibilities
Document Oversight: Manage and organize essential trial documents (e.g., Trial Master File / TMF).
Regulatory Compliance Support: Ensure studies consistently follow guidelines like GCP (Good Clinical Practice), SOPs, and other regulatory requirements.
Audit and Inspection Readiness: Support preparation for audits or inspections from regulators (e.g., MHRA, FDA).
Tracking and Reporting: Monitor compliance metrics, deviations, and quality issues.
Process Improvement: Identify gaps and help improve compliance processes.
Requirements & Qualifications
Previous compliance experience within clinical trials is required.
Fluency in English (candidate must speak English).
Strong knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH).
Degree in life sciences or equivalent industry experience.
Must hold a valid right to work for the country of residence (this role is not eligible for visa sponsorship).
How to Apply
Interested and qualified candidates should apply online by visiting the application link: Apply on IQVIA Workday.
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