Clinical Study Coordinator

Welcome to Henry Ford Health System, where we are dedicated to providing exceptional patient care and advancing medical research. We are currently seeking a highly motivated and organized Clinical Study Coordinator to join our team. In this role, you will have the opportunity to work on groundbreaking clinical trials and contribute to the development of new treatments and therapies. As a Clinical Study Coordinator, you will play a vital role in ensuring the success and ethical conduct of our research studies. We are looking for candidates with a strong background in clinical research, excellent communication skills, and a passion for improving patient outcomes. If you are eager to make a difference in the field of healthcare, we encourage you to apply for this exciting opportunity.

1. Coordinate and manage all aspects of clinical research studies, including recruitment, enrollment, and follow-up of participants.
2. Create and maintain study documents, including protocols, informed consent forms, and study databases.
3. Ensure compliance with all regulatory requirements, including Institutional Review Board (IRB) approvals and Good Clinical Practice (GCP) guidelines.
4. Collaborate with study investigators, sponsors, and other healthcare professionals to ensure timely and accurate completion of study tasks.
5. Conduct study visits and procedures according to protocols and maintain accurate and complete study records.
6. Monitor and report adverse events and protocol deviations in a timely manner.
7. Communicate with study participants, providing education and support throughout the study process.
8. Coordinate study-related meetings and trainings for study team members.
9. Develop and maintain relationships with study sponsors and vendors.
10. Participate in the development and implementation of new research studies and protocols.
11. Keep abreast of new developments and advancements in the field of clinical research.
12. Maintain confidentiality and adhere to all HIPAA regulations.
13. Ensure data integrity and accuracy through regular quality control checks.
14. Contribute to the writing and preparation of study reports and publications.
15. Act as a liaison between the research team and other healthcare professionals involved in the study.
16. Assist with budget and contract negotiations with study sponsors.
17. Train and mentor new staff members and research assistants.
18. Attend conferences and training sessions to improve knowledge and skills related to clinical research.
19. Maintain a safe and clean work environment, adhering to all safety protocols and procedures.
20. Continuously evaluate and improve processes to increase efficiency and effectiveness of study coordination.

According to JobzMall, the average salary range for a Clinical Study Coordinator in Detroit, MI, USA is $45,000 to $70,000 per year. However, this can vary depending on factors such as experience, education, and the specific employer. Some clinical study coordinators in Detroit may earn more or less than this range.

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.