Clinical Study Coordinator- Cancer Clinical and Translational Research Office

Are you passionate about making a difference in the field of oncology research? Do you have strong organizational and communication skills? We are currently seeking a Clinical Study Coordinator to join our Cancer Clinical and Translational Research Office at Henry Ford Health System. In this role, you will play a vital role in coordinating and managing clinical trials for cancer research. The ideal candidate will have a strong background in clinical research, excellent attention to detail, and a desire to contribute to groundbreaking cancer research. If you are ready to join a dynamic team and contribute to cutting-edge research, we encourage you to apply for this exciting opportunity.

1. Coordinate and manage clinical trials: The primary responsibility of the Clinical Study Coordinator will be to oversee the planning, implementation, and management of clinical trials related to cancer research. This will involve working closely with the research team, patients, and other stakeholders to ensure the smooth execution of the trials.
2. Ensure compliance with protocols and regulations: The Clinical Study Coordinator will be responsible for ensuring that all clinical trials are conducted in accordance with established protocols and regulatory requirements. This includes maintaining accurate and up-to-date documentation, maintaining patient confidentiality, and adhering to ethical standards.
3. Recruit and screen patients: The ideal candidate will have strong communication skills to effectively communicate with potential participants and screen them for eligibility. They will also be responsible for obtaining informed consent from participants and enrolling them in the appropriate trials.
4. Collaborate with research team: The Clinical Study Coordinator will work closely with the research team, including principal investigators, physicians, nurses, and other healthcare professionals. They will assist with study design, data collection, and analysis, and provide regular updates on the progress of the trials.
5. Manage study timelines and budgets: The successful candidate will be responsible for developing and maintaining study timelines and budgets, ensuring that trials are completed within the designated timeframe and budget constraints.
6. Maintain accurate records: The Clinical Study Coordinator will be responsible for maintaining accurate and detailed records of all aspects of the clinical trials, including patient information, study protocols, and data collection.
7. Monitor and report adverse events: In the event of adverse events or unexpected outcomes, the Clinical Study Coordinator will be responsible for promptly reporting them to the appropriate parties and taking appropriate action as needed.
8. Ensure quality control: The Clinical Study Coordinator will be responsible for monitoring the quality of data collected during the trials and ensuring that all study procedures are followed accurately and consistently.
9. Train and supervise study staff: The ideal candidate will have excellent organizational skills to manage and train study staff, providing guidance and support as needed to ensure the

According to JobzMall, the average salary range for a Clinical Study Coordinator- Cancer Clinical and Translational Research Office in Detroit, MI, USA is $47,500 - $70,000 per year. However, this salary range can vary depending on factors such as experience, qualifications, and the specific organization or institution hiring for the position.

The Henry Ford Health System is a comprehensive, integrated, non-profit health care organization in Metro Detroit. The corporate office is at One Ford Place, Detroit, Michigan. Henry Ford established the health system in 1915, and it is currently run by a 15-member board of trustees.