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Site Management Expert
2 weeks ago
About the Role
">This is an exciting opportunity to join our site management team as a Clinical Research Associate. In this role, you will be responsible for ensuring the smooth conduct of clinical trials at our partner sites.
">- You will work closely with sites to ensure they are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
- Your primary responsibility will be to perform monitoring and site management work to ensure compliance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- You will also be responsible for creating and maintaining appropriate documentation regarding site management, monitoring visit findings, and action plans.
- Effective communication and problem-solving skills are essential for this role, as you will collaborate and liaise with study team members for project execution support.
What We Offer
">We offer a competitive salary and benefits package, as well as opportunities for career growth and development.
