<p>Clinical Research Coordinator -Oncology</p> <p>On-site 4 days per week</p> <p>Clinical Research Coordinator</p> <p>This role is critical in supporting Oncology clinical trials from initiation through completion, ensuring compliance with regulatory standards and delivering high-quality data</p> <p>Key Responsibilities</p> <p>Coordinate initiation and activation of new clinical trial protocols</p> <p>Prepare study tools (binders, medication diaries, eligibility checklists, flow sheets) using OnCore, Excel, and Word</p> <p>Review patient charts and medical history to confirm protocol eligibility; obtain and maintain source documentation</p> <p>Ensure informed consent is obtained, documented, and filed per IRB guidelines</p> <p>Maintain accurate research records, including consent forms, eligibility documentation, CRFs, and source documents</p> <p>Assist with grading adverse events using NCI toxicity criteria; complete SAE forms per sponsor and regulatory requirements</p> <p>Generate regular reports for tumor study groups and Principal Investigators using OnCore</p> <p>Serve as liaison with study sponsors; schedule monitoring visits and respond to queries promptly</p> <p>Perform blood processing as required for clinical trial protocols</p> <p>Qualifications</p> <p>Bachelor's degree required</p> <p>2+ years of clinical research experience (patient recruitment, data collection, data entry)</p> <p>2+ years of oncology experience (gynecologic oncology experience is a plus)</p> <p>Experience in data management</p> <p>Experience recruiting, screening, and consenting patients for clinical trials</p> <p>Proficiency in multiple EDC systems (Medidata and Inform highly preferred)</p> <p>Familiarity with OnCore and Microsoft Office Suite</p> <p>Blood processing experience</p> <p>Ability to work collaboratively with physicians, nurses, and sponsors</p> <p>Experience with clinical trial coordination and regulatory compliance</p> <p>Familiarity with NCI grading scales and SAE reporting</p> <p>Job Type & Location</p> <p>This is a Contract to Hire position based out of Bronx, NY.</p> <p>Pay and Benefits</p> <p>The pay range for this position is $30.00 - $35.00/hr.</p> <p>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)</p> <p>Workplace Type</p> <p>This is a hybrid position in Bronx,NY.</p> <p>Application Deadline</p> <p>This position is anticipated to close on Dec 16, 2025.</p> <p>About Actalent</p> <p>Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.</p> <p>The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.</p> <p>If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.</p>