Research Protocol Specialist

As a Research Protocol Specialist, you will be instrumental in developing and managing clinical research studies, ensuring regulatory compliance, and facilitating clear communication within medical teams. This role requires a strong foundation in biomedical sciences and practical experience in research protocols.

• *Key Responsibilities:**
• Develop and support clinical research studies, applying scientific and biomedical principles.
• Analyze and interpret research regulations, identifying potential compliance risks in clinical settings.
• Communicate professionally and effectively with physicians and other healthcare personnel regarding research protocols.
• *Required Qualifications:**
• **Education:** Bachelor's or graduate degree in a medical, health, or allied science field from a U.S. Department of Education recognized accredited institution.
• **Experience:** One year of specialized experience, which includes:

* Developing and supporting proposed and active clinical research studies. * Interpreting research regulations and identifying compliance threats in clinical settings. * Communicating professionally with physicians and other healthcare personnel. * *Note: Education cannot be substituted for this specialized experience requirement.*

• *Preferred Qualifications:**
• Certified IRB Professional (CIP) credential.