Clinical Research Coordinator II - Annapolis/Columbia

Overview

We’re looking for passionate and talented professionals to join our team in providing exceptional cancer care. With 15+ locations across Maryland and DC, we offer a dynamic and supportive environment where you can grow and thrive.

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.
• Carefully coordinates patient care in compliance with protocol requirements.
• 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.
• May disburse investigational drug.
• 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.

Qualifications

• Education/Training: Associate's degree in a clinical or scientific related discipline required, Bachelor's degree preferred.
• Minimum three years of experience in a clinical or scientific related discipline required, preferably in oncology.
• SoCRA or ACRP certification preferred.
• Business Experience: Experience in Microsoft Office.
• Experience working with physicians preferred.
• Experience working in clinical research is preferred.
• Specialized Knowledge/Skills: Must have excellent communication skills, strong organizational skills, strong ability to multi-task, excellent time management skills, strong interpersonal skills to be able to interact with multiple people on many different levels, strong attention to detail, and ability to work in a fast-paced environment.