Oncology Clinical Research Coordinator
Job
Actalent
Hinsdale, IL (In Person)
$65,555 Salary, Full-Time
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Job Description
Clinical Research Coordinator (Contract Position)
Contract Duration:
Open-ended (estimated 6 months)Schedule:
40 hours per week, Monday-Friday during standard business hoursLocation:
Onsite Start Date:
ASAP Position Overview We are seeking a detail‑oriented and proactive Clinical Research Coordinator (CRC) to support an ongoing Oncology clinical trial. This contractor will function as one of the primary CRCs for the study and must be able to work independently while managing multiple study activities. The ideal candidate has hands-on clinical research experience, strong organizational skills, and the ability to engage confidently with participants and research staff. Key Responsibilities Participant Recruitment & Screening Identify, recruit, and prescreen potential participants for eligibility. Conduct phone screenings and review inclusion/exclusion criteria. Perform thorough reviews of patient medical records to determine suitability. Participant Interaction & Study Conduct Obtain informed consent from participants in accordance with regulatory and ethical standards. Prepare for study visits, including scheduling participants, confirming informed consent status, preparing documents, and coordinating with the research team. Conduct follow-up communications with participants to ensure retention and protocol compliance. Schedule in-person visits and follow-up appointments; send reminders and information as needed. Data & Documentation Management Collect and enter study data into electronic data capture (EDC) systems with a high degree of accuracy. Create and maintain source documents and ensure all study records are complete, up-to-date, and audit-ready. Resolve EDC data queries promptly. Retrieve necessary medical records and ensure proper documentation. Maintain and organize study binders in compliance with study and regulatory requirements. Ensure adherence to e-diary protocols and assist participants with compliance.Qualifications Clinical Research Experience:
Previous experience as a Clinical Research Coordinator is required. Oncology clinical trial experience requiredTechnical Proficiency:
Experience with electronic medical records (EMR) and electronic data capture (EDC) systems.Communication Skills:
Excellent interpersonal and written communication skills; ability to engage effectively with participants, investigators, and team members. Attention toDetail:
Demonstrated accuracy in documentation, data entry, and protocol adherence. Job Type & Location This is a Contract position based out of Hinsdale, IL. Pay and Benefits The pay range for this position is $25.00 - $35.00/hr. Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan - Pre-tax and Roth post-tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long-term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Hinsdale,IL.
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