Clinical Research Coordinator I, GYN

About the Role

• Responsible for the coordination and administration of multiple research studies.
• Works closely with principal investigators and research staff facilitating all aspects of assigned clinical trials.
• Implements study protocols in accordance with regulatory and institutional requirements.
• Sets up administrative systems to manage the progress of each study.
• Screens, recruits, and follows study participants.
• Collects and reports study data.
• Interacts with study participants diagnosed with various medical conditions and diagnoses.

Key Responsibilities

• Coordinate and administer multiple research studies.
• Facilitate all aspects of assigned clinical trials.
• Implement study protocols.
• Set up administrative systems for study progress.
• Screen, recruit, and follow study participants.
• Collect and report study data.
• Interact with study participants compassionately and respectfully.

Requirements & Tech Stack

• Bachelor’s degree required.
• Experience with computer systems, including web-based applications.

Qualifications

• 0-2 years of experience in a research or medical setting.
• Ability to address problems that are routine, somewhat repetitive, and generally solved by following clear directions and procedures.
• Ability to travel nationally to other research sites, attend investigator meetings and educational conferences as required.
• Strong organizational, multi-tasking, attention to detail, and communication skills.
• Ability to take direction, set priorities, and work somewhat independently.
• Ability to demonstrate a positive attitude and respond to requests in a timely and respectful manner.
• Ability to work in small teams and interact with professional personnel at all levels of an organization.
• In the absence of any required skills, demonstrates the ability to be thoroughly trained to meet organizational standards.
• Must be vaccinated against influenza (flu) as a condition of employment.