The US Oncology Network · 22 hours ago
Clinical Research Coordinator II
Rockville, CT
Full-time
Onsite
Mid Level
$58K/yr - $89K/yr
3+ years expThe US Oncology Network is dedicated to providing exceptional cancer care, and they are seeking a Clinical Research Coordinator II to join their team. This role involves recruiting, screening, consenting, and enrolling patients in clinical trials while ensuring compliance with protocol requirements and regulatory standards.
CommunitiesHealth CareMedicalOncologyTest and Measurement
Responsibilities
Screens potential participants for protocol eligibility. Presents trial concepts and details to participants, participates in the informed consent process, and enrolls participants into clinical trials
Coordinates participant care in compliance with protocol requirements. May disburse investigational product and maintain accountability records. Oversees preparation of orders by providers to ensure protocol compliance. Packages and ships laboratory specimens to central vendors as applicable. Completion of Hazmat and/or IATA training may be required
In collaboration with providers, reviews participants for changes in condition, adverse events, concomitant medications, protocol compliance, and response to study treatment. Thoroughly documents all findings and participates in data collection
Prepares study‑related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports
Maintains regulatory documents in accordance with organizational SOPs and applicable regulations. May assist with scheduling monitoring and auditing visits, and interact with monitors/auditors as needed. May collaborate with research leadership in study selection processes
Participates in required training and education programs. May contribute to education of clinical staff regarding research procedures. Works with staff to develop action plans and performance improvement initiatives to enhance quality
May compile and report protocol activity, enrollment trends, data entry compliance, and research financial information to practice leadership and providers. May review protocol‑specific billing guides and submit billing information to the appropriate personnel
Qualification
Required
Associate's degree in a clinical or scientific discipline
Minimum three years of experience in a clinical or scientific field
Experience with Microsoft Office applications
Excellent communication skills
Strong organizational abilities
Ability to multi‑task effectively
Strong time‑management skills
High level of interpersonal skills to interact with individuals at various levels
Strong attention to detail
Ability to work in a fast‑paced environment
May be responsible for basic clinical assessments
Preferred
Bachelor's degree
SoCRA or ACRP certification
Experience working with physicians
Experience in clinical research
Company
The US Oncology Network
Every day, The US Oncology Network helps approximately 3,300 providers deliver value-based, integrated care for patients—close to home.
10001+ employees
Funding
Current Stage
Late StageTotal Funding
unknown2010-12-30Acquired
Leadership Team
R. Steve Paulson
National Policy Board Executive Committee
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