Clinical Research Coordinator: Lead Cancer Trials & Care

US Oncology Network-wide Career Opportunities; Washington (District of Columbia); On-site; USD 52,000 - 89,000; Full time

Job summary

Maryland Oncology Hematology is seeking a dedicated clinical research professional to support multiple oncology trials. You will screen potential participants, obtain consent, and help ensure protocol compliance across sites with supervision from physicians and research staff.

This role requires an Associate degree (Bachelor preferred), at least three years in a clinical setting, and comfort with regulatory duties, data entry, and training in GCP and SOPs.

Qualifications

• Associate degree in clinical or scientific field required; Bachelor's degree preferred.
• Minimum three years of experience in a clinical or scientific field.
• SoCRA or ACRP certification preferred.
• Experience with Microsoft Office applications.
• Experience working with physicians preferred.
• Experience in clinical research preferred.

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.
• 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, 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.

Skills

Excellent communication

Organizational skills

Multitasking

Time management

Interpersonal skills

Attention to detail

Fast-paced work

Clinical assessments (basic)

Education

Associate's degree in clinical or scientific discipline

Bachelor's degree preferred

SoCRA or ACRP certification preferred

Tools

Microsoft Office

Job description

Maryland Oncology Hematology is seeking a dedicated clinical research professional to support multiple oncology trials. You will screen potential participants, obtain consent, and help ensure protocol compliance across sites with supervision from physicians and research staff.

This role requires an Associate degree (Bachelor preferred), at least three years in a clinical setting, and comfort with regulatory duties, data entry, and training in GCP and SOPs.