Job Title: Clinical Research Coordinator

Job Description

This role involves direct patient interaction, screening and recruitment, managing source documentation, and documenting in electronic medical records (EMR). You will be responsible for ordering labs and ensuring protocol compliance. While data entry is managed by a separate team, you will work closely with patients enrolled in oncology trials, guiding them through their therapy journey.

Responsibilities

• Screen, consent, and enroll patients in oncology trials.
• Monitor patients throughout their therapy, ensuring protocol compliance.
• Collaborate with clinic staff to schedule appointments, including EKGs and vitals.
• Interact with nursing staff, medical assistants, and clinical team for insurance authorizations.
• Work alongside infusion nurses to schedule treatment appointments.
• Maintain a patient-focused approach with enthusiasm and dedication.
• Ensure research procedures outside clinical norms are completed accurately and timely.

Essential Skills

• Minimum of 2 years of clinical research coordinator experience.
• Proficiency in clinical research, pre-screening patients, oncology chart review, and patient recruitment.
• Bachelor's degree in a relevant field.

Additional Skills & Qualifications

• Experience with patient study enrollment is required.
• Ability to read protocols, identify side effects, and assist patients in managing them.
• Strong organizational skills.
• Tuition reimbursement available.
• ACRP membership fees and conference attendance may be sponsored.

Work Environment

The role allows the CRC to engage in cutting-edge oncology research. Trials include pharmaceutical-sponsored Phase I and II, investigator-led trials, and cooperative group trials. You will work within disease-specific teams in the cancer center, collaborating with data management staff. The position is full-time, Monday to Friday, 8 AM to 5 PM, with some flexibility based on clinic schedules. Office visits require daily on-site presence.