
Senior Oncology Clinical Research Professional
2 semanas atrás
Sr. Clinical Research Associate
- Oncology Expertise Required
We are seeking a highly experienced Senior Clinical Research Associate to lead site management and monitoring visits in the oncology field.
About the Role:
The ideal candidate will possess at least 2 years of on-site monitoring experience in oncology, with a strong background in clinical research regulatory requirements, Good Clinical Practice (GCP), and International Conference on Harmonization (ICH) guidelines.
Key Responsibilities:
- Perform site monitoring visits, adapting and driving subject recruitment plans to enhance predictability.
- Administer protocol and related study training to assigned sites, establishing regular communication to manage ongoing project expectations.
- Evaluate the quality and integrity of study site practices, escalating quality issues as appropriate.
- Manage study progress by tracking regulatory submissions, recruitment, enrollment, and data query generation and resolution.
Requirements:
A Bachelor's Degree in a scientific discipline or healthcare is preferred. Additional responsibilities include creating and maintaining documentation regarding site management, monitoring visit findings, and action plans.
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