Impact-Driven Clinical Trials Coordinator

Sarah Cannon Research Institute; Nashville (TN); On-site; USD 65,000 - 90,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) seeks a Study Coordinator to plan and monitor complex Phase I–IV clinical protocols. You will abstract, assemble, and organize data while ensuring protocol adherence and reporting for the study team.

You will work with the physician PI, data operations managers, sponsor, and study staff to drive trial startup, execution, and close-out across multiple sites.

Qualifications

• An understanding of clinical trial data.
• Knowledge of FDA guidelines and GCP is required.
• The ability to work independently in a fast paced environment.
• Interpersonal skills, detailed-oriented and meticulous.
• Computer skills with ability using clinical trial databases, electronic data capture, MS Access or Excel
• Bachelor Degree is preferred.
• At least one year of experience in healthcare, research or other science related field.
• At least one year of experience planning and managing clinical trial process.

Responsibilities

• Lead the execution of trials for the research team.
• Track all assigned clinical activity in startup, interim and close out lifecycles.
• Confirm patient eligibility and discuss discrepancies with nursing staff and physicians.
• Verify study procedures are performed within the protocol windows.
• Participate in sponsor teleconferences and update study staff.
• Present at weekly protocol meetings to investigators and management.
• Monitor safety data and report adverse events per protocol.

Skills

Clinical trials

FDA guidelines

GCP

Independent work

Data management

MS Access

Excel

Education

Bachelor Degree

Tools

MS Access

Excel

EDC / Electronic Data Capture

Job description

Sarah Cannon Research Institute (SCRI) seeks a Study Coordinator to plan and monitor complex Phase I–IV clinical protocols. You will abstract, assemble, and organize data while ensuring protocol adherence and reporting for the study team.

You will work with the physician PI, data operations managers, sponsor, and study staff to drive trial startup, execution, and close-out across multiple sites.