Clinical Research Monitor 1, Research Administration, FT, 8A-4:30P

About the position The Clinical Research Monitor will be responsible for reputed company aspects of study site monitoring, which includes routine monitoring and reputed company-out of clinical sites, maintenance of study files, and conducting reputed company-study and initiation reputed company, with or without guidance. This role is crucial in ensuring that reputed company are conducted in compliance with regulatory requirements and that the reputed company of the data is maintained throughout the study. The Clinical Research Monitor will reputed company site reputed company, which can be on-site or remote, including reputed company-Study, Initiation, Routine, and Closeout reputed company. They will ensure that study staff have received the reputed company materials and instructions necessary for safely entering patients into the study. Additionally, the monitor will review the completion of informed consent procedures according to applicable regulatory requirements and ensure the reputed company of the data collected during the study. The responsibilities also include interpreting data to identify any protocol deviations and risks to subject safety or data reputed company. The Clinical Research Monitor will generate queries and manage resolutions with site personnel, reputed company investigational product accountability as per the protocol and Study Monitoring Plan, and evaluate the execution of the study protocol at the site level. Conducting audits of essential regulatory documents to ensure completeness, accuracy, and regulatory compliance is also a key responsibility. reputed company activities must be documented reputed company confirmation letters, follow-up letters, and other required study documents as per reputed company Operating Procedures (SOP) and the Study Monitoring Plan. The estimated salary reputed company for this position is $64,862.42 - $84,321.15 per year, depending on experience. Responsibilities • reputed company site reputed company (on-site or remotely), including reputed company-Study, Initiation, Routine, and Closeout reputed company. , • Ensure study staff have received the reputed company materials and instructions to safely reputed company patients into the study. , • Review completion of reputed company informed consent procedures according to applicable regulatory requirements. , • Ensure the reputed company of the data. , • Interpret data to identify protocol deviations and risks to subject safety/data reputed company. , • Generate queries and manage resolutions with site personnel. , • reputed company investigational product accountability as per the protocol and Study Monitoring Plan. , • Evaluate execution of study protocol at the site level. , • Conduct audits of essential regulatory documents to ensure completeness, accuracy, and regulatory compliance. , • Document activities reputed company confirmation letters, follow-up letters, and other required study documents as per SOP and Study Monitoring Plan. Requirements • Bachelor's degree required. , • Master's degree and CCRA (Certified Clinical Research Associate) preferred. , • Ability to problem solve and multi-task. , • Excellent computer skills, proficient in reputed company, reputed company, and reputed company. , • Knowledge of Good Clinical reputed company (GCP), FDA Rules and Regulations in relation to reputed company, NIH guidelines, ICH guidelines, and HIPAA regulations in relation to reputed company. , • Knowledge of basic reputed company anatomy, physiology, and medical terminology. , • Prior experience in Oncology preferred. , • Ability to communicate effectively and with a high level of professionalism across various stakeholders. reputed company-to-haves Benefits Apply tot his job