Oncology Research Coordinator – Clinical Trials Impact

1100 Endeavor Health Clinical Operations; Evanston (IL); On-site; USD 35,000 - 52,000; Full time

Benefits offered by this job

Career growth opportunities

Medical, dental, vision options

Tuition reimbursement

Free parking

Wellness program

Savings plan

Health savings account

Retirement with company match

Paid time off

Community involvement

Job summary

Endeavor Health's Evanston, IL-based Research Coordinator-Oncology role is a full/part-time position. The role focuses on consenting and treating patients, recruiting for trials, managing medical histories, handling lab samples, and dispensing study drugs per protocol.

You will use electronic capture systems, prepare for audits, and ensure regulatory compliance across study activities. The position requires a high school diploma (bachelor’s preferred) and 1–5 years of research experience, with

Qualifications

• Education: High School diploma required; Bachelor’s degree preferred in healthcare sciences.
• Experience: 1-5 years of research experience.

Responsibilities

• Provides clinical care services including consenting, treating and monitoring of patients
• Recruit and screen candidates for clinical trials
• Acquire past medical and medication history profiles
• Obtain, process and ship biological lab samples
• Dispense research drug to patients according to protocol.
• Utilize electronic capture to submit and update patient information.
• Prepare for routine audits and oversight visits
• Perform a variety of research, data entry and regulatory duties of a routine and technical nature within the required time frames
• Ensure adherence to protocols and quality of information received
• Identifying and screening study participants, enroll subjects to the trials in adherence with the protocol
• Assist with developing study budget proposals and tracking study expenditures
• Assist with study time reporting
• Ensure compliance with local, state and Federal regulations for the protection of human subjects
• Complete regulatory submissions/revisions for the Institutional Review Board (IRB)
• Communicate and coordinate with physicians, division staff, and other departmental study personnel as required for study design, implementation and completion
• Complete data abstraction and data entry for study specific databases.
• Review and timely report study related adverse events to the sponsor.

Education

High School diploma

Bachelor’s degree (preferred)

Job description

Endeavor Health's Evanston, IL-based Research Coordinator-Oncology role is a full/part-time position. The role focuses on consenting and treating patients, recruiting for trials, managing medical histories, handling lab samples, and dispensing study drugs per protocol.

You will use electronic capture systems, prepare for audits, and ensure regulatory compliance across study activities. The position requires a high school diploma (bachelor’s preferred) and 1–5 years of research experience, with