Clinical Oncology Research Specialist

Oncology Clinical Research Professional As a critical member of our team, you will be responsible for overseeing the conduct of clinical trials at investigator sites.

This includes site selection, initiation, monitoring, and close-out visits to ensure compliance with ICH Good Clinical Practice (ICH GCP) and FDA regulations.Key Responsibilities : Perform site selection, initiation, monitoring, and close-out visits of investigational sites for a portfolio of clinical trials in oncology settings.Manage the progress of assigned sites by tracking patient recruitment and enrollment, CRF completion and submission, source data verification, data collection, and data query generation and resolution.Conduct monitoring activities, including source data review and verification, essential documentation review and reconciliation, Investigational Product (IP) management and accountability, and lab / kit supply management.You will work closely with investigative sites and personnel to develop collaborative relationships and maintain communication through frequent contact to ensure site compliance, adequate enrollment, and understanding of study requirements.Requirements : Bachelor's degree in life science / biomedical / medical science with proficient knowledge of clinical / scientific terminology and methods common to oncology therapeutic settings.2+ years of clinical research experience, preferably in early phase oncology.Strong communication and interpersonal skills, with ability to independently prioritize tasks and manage time effectively.Our company is a leading biopharmaceutical organization dedicated to developing innovative cell therapies for serious diseases.

We are trailblazers in the field of AL Amyloidosis and other complex conditions, with a focus on delivering effective solutions for patients.