On-Site Study Coordinator

About the role

The On-Site Study Coordinator/Research Assistant position is responsible for the coordination and support of remote site activities for assigned projects. This role works closely with the Principal Investigator and other members of the study team to ensure smooth execution of clinical trials.

Responsibilities

• Serve as point of contact for day-to-day Site communications, document submissions and activity coordination.
• Support pre-screening, screening and recruitment activities, as assigned.
• Responsible for subject re-consenting, acquiring medical records, conducting protocol activities, as directed by the Principal Investigator.
• Perform data-entry, evaluate and respond to system queries and monitor clinical databases as assigned.
• Establish and maintain timely Site communication as assigned.
• Maintain documentation which complies with IRB/FDA policies.
• Assist with study closeout.
• Aid site with other study-related activities as directed.

Requirements

• Bachelor’s degree or equivalent experience defined as a minimum of 2 years related, combined experience in education, knowledge and skills that will allow one to perform the tasks of the role proficiently.
• Minimum 2 years of study coordinator experience.

Skills

• Ability to manage technology and web-based research platforms on PC (Microsoft OS) laptop in the remote workspace; Study Team experience is ideal.
• Critical thinking skills.
• Strong communication Skills (verbal and written).
• Ability to work independently, and collaboratively with other CSCs to delegate tasks as needed.
• Ability to work independently and as a team member.
• Able to work independently and as a team member.
• Able to take initiative while following directives.