Compliance Clinical Trials Assistant

Leiden, Netherlands \| Full time \| Home\-based \| R1547056

We are seeking an experienced Compliance Clinical Trials Assistant to join our cFSP (sponsor\-dedicated) team in EMEA.
Candidates are required to have previous compliance experience within clinical trials to be considered.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.
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Deze vacature komt van indeed. Originele vacature bekijken ↗