State Licensed Senior Clinical Research Coordinator

A company is looking for a Senior Clinical Research Coordinator (Oncology).

Key Responsibilities

Implement and monitor clinical trials and research projects, ensuring compliance with protocol and sponsor requirements

Identify and report adverse events and protocol deviations, while maintaining communication with community agencies and study sponsors

Coordinate multidisciplinary teams, ensuring adequate training and resources for research protocol procedures

Required Qualifications

Bachelor's degree in science, healthcare, or related fields; equivalent experience may be considered

Clinical Research Coordinator professional certification is required

Minimum of 4 years of experience as a lead coordinator in clinical trials, with at least 10 drug or device trials

Experience in startup, recruiting, and implementation of research protocols and clinical trials processes

Proficiency in using electronic data capture software and Clinical Trial Management Systems (CTMS)