Simran Toor

I am a Clinical Research Associate with over two years of experience in clinical trial coordination, regulatory documentation, and patient data management. My journey in the healthcare sector has equipped me with a robust understanding of clinical operations, and I am passionate about contributing to the success of clinical trials. I thrive in collaborative environments where I can leverage my organizational strengths and cross-functional communication skills.

At Memorial Sloan Kettering Cancer Center, I support the execution of clinical studies across various phases, ensuring compliance with ICH-GCP and FDA regulations. I manage the Trial Master File (TMF) and maintain essential documents, facilitating seamless communication among multidisciplinary teams. My proactive approach to data verification and query resolution has been instrumental in ensuring audit readiness and adherence to protocols.

My previous roles have honed my skills in clinical trial documentation and patient screening activities, where I actively contributed to process improvement efforts. I am now seeking a Clinical Trials Associate position where I can apply my hands-on approach to support clinical operations and advance trial success.