Remote-Ready Clinical Research Coordinator I

aoncology; Indianapolis (IN); On-site; USD 27,083 - 47,651; Full time

Job summary

Hematology Oncology of Indiana is seeking a Clinical Research Coordinator I (non-RN) to support the performance and ongoing management of research studies under the PI's supervision.

The role covers entry-level protocol design and procedures, overseeing 5 open trials annually and 2–10 patients on study treatment. Strong regulatory knowledge, data integrity, and communication skills are essential for compliant, efficient trial operations.

Qualifications

• High school education required.
• Some college is preferred.
• Prior research or related medical science experience.

Responsibilities

• Responsible for the performance of the research study under the medical supervision of the Principal Investigator.
• The Clinical Research Coordinator I (non-RN) is responsible for the overall successful implementation and ongoing management of the research studies.
• Ability to perform basics tasks and exhibit the knowledge of key aspects of clinical research at an essential or foundational level.
• Primary responsibility includes study designs with entry-level complexity (phase 4, observational/registry trial design) and associated study procedures.
• Administratively and clinically manage an average 5 clinical trials open to accrual annually and/or active (on study treatment) patient volume 2-10 annually.
• Demonstrates working knowledge of all facets of role, relevant regulations, and organizational and departmental policies and procedures.
• Performs other duties and projects as assigned. Performs all duties in accordance with regulatory requirements and organizational policies and procedures.

Skills

Analysis & Critical Thinking

Interpersonal Effectiveness

Communication Skills

Customer Service & OrganizationalAwren

Self-Management

Education

High school education

Some college

Tools

MS Office Suite (Word, Excel, PowerPoint, Outlook)

EMR systems

EDC (Electronic Data Capture)

CTMS

Job description

Hematology Oncology of Indiana is seeking a Clinical Research Coordinator I (non-RN) to support the performance and ongoing management of research studies under the PI's supervision.

The role covers entry-level protocol design and procedures, overseeing 5 open trials annually and 2–10 patients on study treatment. Strong regulatory knowledge, data integrity, and communication skills are essential for compliant, efficient trial operations.