Clinical Research Coordinator * Oncology clinical research experience preferred *
$70,482–$74,794 year
On-siteNew York, United States
Job Summary
Coordinate oncology clinical trials from research planning through patient follow-up, managing recruitment, pre-screening, informed consent, and eligibility processes under investigator supervision. Prepare for study visits by ordering biospecimens, laboratory tests, and EKGs, while tracking patient assignments and monitoring infusion chair schedules. Maintain active trial trackers, compile weekly treatment lists, and ensure protocol compliance through self-audits and adherence to Good Clinical Practice guidelines. Support study activation, feasibility assessments, and external audits, and train junior coordinators on study operations and system usage.
Required Qualifications
- Bachelor's Degree or equivalent combination of education and experience
- 2 years relevant experience
- Computer literate
- Good interpersonal, writing and verbal communication skills
- Effective oral, written, communication, interpersonal skills
- Ability to identify, analyze and solve problems
- Time management skills and ability to work well under pressure
- Proficiency in using various Microsoft Office applications such as Word, Excel, Access, PowerPoint and Outlook
- Familiar with Internet applications
- Moderate competency in medical terminology
- Good Clinical Practice (GCP) guidelines
- Federal Regulation that govern the conduct of human subjects research
- Institutional Review Board and institutional policies and procedures related to human subjects research
- Ability to manage priorities and deadlines and maintain service level expectations for tasks
- Must be able to work under the direction of supervision
Desired Qualifications
- Oncology clinical research experience
- 3 years experience in research or related experience
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