Compliance Clinical Trials Assistant
Posted:
Company Details
Name:IQVIA
Industry:
Hospital & Health Care
Website:
https://www.iqvia.com/
Description:
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 …
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Job Details
Job Type:
Full Time
Workplace Type:
On-site
Qualification:
Diploma
Job Experience:
Mandatory
Job Location:
Nairobi County, Kenya
Closing Date:
Undisclosed
Salary:
Undisclosed
Other Pay:
Benefits
Job Category:
Others
Job Description
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.
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