Clinical Research Coordinator

Attention all clinical research professionals! Are you passionate about advancing medical knowledge and improving patient care? Novant Health is seeking a highly skilled Clinical Research Coordinator to join our dynamic team. As a Coordinator, you will play a crucial role in the execution of clinical trials, ensuring compliance with regulations and protocols. This is an exciting opportunity to be part of groundbreaking research that has the potential to positively impact countless lives. If you have a strong background in clinical research, excellent organizational skills, and a desire to make a difference, we want to hear from you!

1. Oversee and manage the execution of clinical trials, ensuring adherence to regulations and protocols.
2. Coordinate and facilitate communication between research team members, sponsors, and regulatory agencies.
3. Monitor and track study progress and data collection, ensuring accuracy and completeness.
4. Prepare and submit all necessary documentation for institutional review board (IRB) approval and regulatory compliance.
5. Organize and maintain study records and data in a timely and organized manner.
6. Develop and maintain strong relationships with study participants, ensuring their safety and well-being throughout the trial.
7. Educate and train study team members on protocol requirements and ensure compliance.
8. Collaborate with physicians and other healthcare professionals to ensure effective patient enrollment and study participation.
9. Conduct study-related procedures and assessments, adhering to Good Clinical Practice (GCP) guidelines.
10. Monitor and report any adverse events or protocol deviations to the appropriate parties.
11. Assist in the development and implementation of study protocols and procedures.
12. Participate in study meetings and provide updates on study progress and results.
13. Remain current on industry trends and regulations related to clinical research.
14. Contribute to the development and improvement of research processes and procedures.
15. Act as a liaison between the research team and other departments within the organization.
16. Maintain confidentiality and abide by ethical standards in all aspects of the job.
17. Collaborate with study sponsors and vendors to ensure timely and efficient study execution.
18. Proactively identify and address any issues or challenges that may arise during the course of the study.
19. Comply with all safety and health regulations, policies, and procedures.
20. Demonstrate a strong commitment to patient safety and ethical research practices.

According to JobzMall, the average salary range for a Clinical Research Coordinator in Charlotte, NC, USA is between $42,000 and $70,000 per year. This range can vary depending on factors such as experience, education, and specific job responsibilities. Some employers may also offer additional benefits and bonuses, which can affect the overall compensation package.

Novant Health is a four-state integrated network of physician clinics, outpatient centers and hospitals. Its network consists of more than 1,600 physicians and 29,000 employees at more than 640 locations, including 15 medical centers and hundreds of outpatient facilities and physician clinics.