Maryland Oncology Hematology ยท 2 weeks ago
Clinical Research Coordinator II - White Oak
White Oak, NC
Full-time
Onsite
Mid Level
$58K/yr - $89K/yr
3+ years expMaryland Oncology Hematology is seeking passionate and talented professionals to join their team in providing exceptional cancer care. The Clinical Research Coordinator II will be responsible for recruiting and enrolling patients in clinical trials, coordinating patient care, and ensuring compliance with protocol requirements.
Health CareHospitalMedicalOncology
Responsibilities
Screens potential patients for protocol eligibility. Presents trial concepts and details to the patients, participates in the informed consent process, and enrolls patients on clinical trials
Coordinates patient care in compliance with protocol requirements. May disburse investigational drug. Maintains investigational drug accountability. Oversees the preparation of orders by physicians to assure that protocol compliance is maintained. Packages and ships lab specimens to central vendors where applicable. Required to complete Hazmat and/or IATA training
In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings and participates in data collection of all subjects
Responsible for preparing study-related documentation such as protocol worksheets, adverse event reports, institutional review board documents, and annual continuing review reports
Maintains regulatory documents in accordance with USOR SOP and applicable regulations. May participate in scheduling monitoring and auditing visits, as well as interact with the monitors/auditors while onsite. May collaborate with Research Site Leader in the study selection process
Participates in required training and education programs. May be responsible for education of clinic staff regarding clinical research. Collaborates with staff in the development of action plans and performance improvement opportunities with staff to improve quality
May be responsible for compiling and reporting protocol activity, accrual trends, data entry compliance, and research financial information to practice administration and physicians. May be responsible for reviewing protocol specific billing guides and submitting billing information to appropriate personnel
Qualification
Required
Associate's degree in a clinical or scientific related discipline required
Minimum three years of experience in a clinical or scientific related discipline required
Experience in Microsoft Office
Must have excellent communication skills
Excellent organizational skills
Strong ability to multi-task
Excellent time management skills
Must have strong interpersonal skills to be able to interact with multiple people on many different levels
Must have a high level of attention to detail
Must be able to work in a fast-paced environment
This position requires a self-motivated individual who can work independently and manage priorities effectively in a fast-paced environment
Preferred
Bachelor's degree preferred
SoCRA or ACRP certification preferred
Experience working with physicians preferred
Experience working in clinical research is preferred
Company
Maryland Oncology Hematology
Maryland Oncology Hematology is a community based healthcare institution specialized in research and treatment of cancer patients.
501-1000 employees
Funding
Current Stage
Late StageLeadership Team
David Weng
Partner
Recent News
Maryland Daily Record
2024-12-17
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