Clinical Research Site Lead

American Oncology Management Company; Indianapolis (IN); On-site; USD 85,000 - 110,000; Full time

Job summary

Hematology Oncology of Indiana seeks a Research Site Manager to lead day-to-day site activities, drive trial performance, and work with leaders to solve issues impacting goals. You will oversee trials, ensure high-quality data, manage regulatory submissions, and supervise the clinical research coordinator team to support patient care in investigational studies.

Strong knowledge of FDA/IRB requirements and budgeting, staffing, and purchasing is required, with 2+ years in healthcare/research and

Qualifications

• Minimum 2 years of experience in healthcare and research.
• Experience with oncology clinical trials.
• Familiarity with FDA, IRB, and regulatory requirements.

Responsibilities

• Lead the implementation of clinical trials and manage site start-up and enrollment.
• Supervise the clinical research coordinator team handling screening, enrollment, and patient care.
• Ensure high-quality data collection and timely regulatory submissions to IRB.
• Oversee site operations, budgeting, and resource planning following CMS rules.

Skills

Leadership

Communication

Problem solving

Time management

Education

Bachelor's degree in Biological Science/Healthcare or related field

Tools

MS Office

Clinical trial management software

Job description

Hematology Oncology of Indiana seeks a Research Site Manager to lead day-to-day site activities, drive trial performance, and work with leaders to solve issues impacting goals. You will oversee trials, ensure high-quality data, manage regulatory submissions, and supervise the clinical research coordinator team to support patient care in investigational studies.

Strong knowledge of FDA/IRB requirements and budgeting, staffing, and purchasing is required, with 2+ years in healthcare/research and