Clinical Research Coordinator

Are you looking for a challenging and rewarding career in clinical research? Join the prestigious Yale University as a Clinical Research Coordinator and play a crucial role in advancing medical knowledge and improving patient outcomes. As a coordinator, you will work closely with researchers, healthcare professionals, and patients to facilitate and coordinate clinical trials. We are seeking a highly organized and detail-oriented individual with a passion for healthcare and research. If you are ready to make a difference in the world of medicine, we invite you to apply for this exciting opportunity.

1. Coordinate and facilitate clinical trials: The primary responsibility of the Clinical Research Coordinator is to oversee and manage all aspects of clinical trials. This includes coordinating with researchers and healthcare professionals to ensure smooth implementation of the trial, managing patient recruitment and enrollment, and organizing study procedures and timelines.
2. Communicate with stakeholders: The coordinator will be responsible for maintaining effective communication with various stakeholders including researchers, healthcare professionals, patients, and other team members. This may involve providing updates on study progress, addressing any concerns or issues, and ensuring all parties are well-informed throughout the duration of the trial.
3. Ensure compliance: The coordinator will be responsible for ensuring that all clinical trials are conducted in compliance with relevant regulations, protocols, and ethical standards. This may involve obtaining necessary approvals, maintaining accurate records, and monitoring and reporting any deviations from the protocol.
4. Manage study materials and resources: The coordinator will be responsible for managing all study materials and resources including study documents, equipment, and supplies. This may involve coordinating with vendors, ordering and tracking supplies, and maintaining inventory.
5. Collect and analyze data: The coordinator will work closely with researchers to collect and analyze data from clinical trials. This may involve administering questionnaires, conducting interviews, and collecting biological samples from study participants.
6. Organize and maintain study records: It is crucial for the coordinator to maintain accurate and up-to-date records of all study activities. This includes keeping track of study participants, study procedures, and any changes or updates to the study protocol.
7. Ensure participant safety and confidentiality: The coordinator will play a key role in ensuring the safety and well-being of study participants. This includes maintaining confidentiality of participant information and promptly addressing any adverse events or concerns.
8. Support research team: The coordinator will provide administrative and logistical support to the research team as needed. This may include scheduling meetings, preparing study materials, and assisting with data management and analysis.
9. Stay updated on industry trends and regulations: The coordinator will be

According to JobzMall, the average salary range for a Clinical Research Coordinator is $45,000 to $65,000 per year. However, salaries can vary depending on factors such as location, experience, and the specific industry the coordinator is working in. Some coordinators may earn as much as $80,000 or more, while others may earn closer to $30,000. Factors such as education, certifications, and job responsibilities may also impact the salary range for a

Yale University is a private Ivy League research university in New Haven, Connecticut. Founded in 1701, it is the third-oldest institution of higher education in the United States and one of the nine Colonial Colleges chartered before the American Revolution. Yale is ranked as one of the top universities in the world.