Clinical Research Coordinator

What they do

• Overseeing the smooth running of clinical trials.
• Collecting, coding and analyzing data obtained from research.
• Managing research budgets.
• Informing participants about study objectives.
• Administering questionnaires.
• Monitoring research participants to ensure adherence to study rules.
• Adhering to research regulatory standards.
• Adhering to ethical standards.
• Maintaining detailed records of studies as per FDA guidelines, including things such as drug dispensation.
• Liaising with laboratories regarding findings.
• Participating in subject recruitment efforts.
• Ensuring that the necessary supplies and equipment for a study are in stock and in working order.
• Engaging with subjects and understanding their concerns.

Qualifications

• Associates degree in Nursing or related field.
• + years in healthcare.
• Analytical mindset.
• Attention to detail.
• Exceptional interpersonal skills.
• Outstanding written and verbal communication.
• Excellent organizational skill.
• Willingness to continually self-educate.