Oncology Clinical Trials Study Coordinator - Lead Research

McKesson; Nashville (TN); On-site; USD 52,000 - 75,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) seeks a Study Coordinator to plan, monitor, and execute complex Phase I–IV clinical research protocols. You will abstract and organize data, ensure adherence to the protocol, and prepare reports for investigators and sponsors.

You will work with physicians, data operations managers, and study teams to drive trial activities, verify eligibility, and discuss discrepancies with nursing staff.

Qualifications

• Understanding of clinical trial data.
• Knowledge of FDA guidelines and GCP.
• Ability to work independently in a fast paced environment.
• Interpersonal skills, detailed-oriented and meticulous.
• Computer skills using clinical trial databases, electronic data capture, MS Access or Excel.
• Bachelor Degree preferred.
• At least one year of healthcare, research or related field experience.
• At least one year of planning and managing clinical trial processes.

Responsibilities

• Plan and monitor the execution of complex Phase I–IV clinical research protocols.
• Abstract, assemble and organize research data while monitoring adherence to protocols and preparing reports.
• Lead execution of trials for the research team and coordinate with investigators and sponsors.
• Plan and track all assigned clinical activity across startup, interim, and close-out phases.
• Verify patient eligibility and discuss discrepancies with nursing staff and physicians.
• Ensure study procedures are performed within protocol-specified windows.
• Participate in sponsor teleconferences and update on patient visits and toxicity.

Skills

Clinical trial data

FDA guidelines

GCP

Independent work

Interpersonal skills

MS Access

Excel

Clinical trial databases

Data entry

Trial process planning

Education

Bachelor's degree

Tools

MS Access

Electronic Data Capture

Job description

Sarah Cannon Research Institute (SCRI) seeks a Study Coordinator to plan, monitor, and execute complex Phase I–IV clinical research protocols. You will abstract and organize data, ensure adherence to the protocol, and prepare reports for investigators and sponsors.

You will work with physicians, data operations managers, and study teams to drive trial activities, verify eligibility, and discuss discrepancies with nursing staff.