IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services,...

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Compliance Clinical Trials Assistant

Job Type

Full Time

Qualification

BA/BSc/HND

Experience

Location

Nairobi

Job Field

Risk Management and Compliance

Key Responsibilities

• Document oversight - managing and organising essential trial documents (e.g., Trial Master File / TMF)
• Regulatory compliance support - ensuring studies follow guidelines like GCP (Good Clinical Practice), SOPs, and regulatory requirements
• Audit and inspection readiness - supporting preparation for audits or inspections from regulators (e.g., MHRA, FDA)
• Tracking and reporting - monitoring compliance metrics, deviations, and quality issues
• Process improvement - identifying gaps and helping improve compliance processes

What We’re Looking For

• Previous compliance experience within clinical trials required.
• Candidate must speak English
• 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.

Please note: This role is not eligible for visa sponsorship and candidates must hold valid right to work for country of residence.

• Document oversight - managing and organising essential trial documents (e.g., Trial Master File / TMF)
• Regulatory compliance support - ensuring studies follow guidelines like GCP (Good Clinical Practice), SOPs, and regulatory requirements
• Audit and inspection readiness - supporting preparation for audits or inspections from regulators (e.g., MHRA, FDA)
• Tracking and reporting - monitoring compliance metrics, deviations, and quality issues
• Process improvement - identifying gaps and helping improve compliance processes

• Previous compliance experience within clinical trials required.
• Candidate must speak English
• 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.