Oncology Clinical Trials Coordinator

Nebraska Hematology Oncology; Lincoln (NE); On-site; USD 65,000 - 85,000; Full time

Job summary

Nebraska Hematology-Oncology, PC. is seeking a Clinical Trials Coordinator to support multi-study oncology/hematology trials. You will manage regulatory processes, patient visits, and data entry under the supervision of the Clinical Trials Manager.

Responsibilities include initiating studies, coordinating with investigators, ensuring SOP compliance, and maintaining study materials and communications with sponsors and the care team.

Qualifications

• Detail-oriented with excellent communication skills.
• Knowledge of organizational policies, regulations, and procedures to administer clinical research protocols.
• Knowledge of medical terminology and safety requirements.
• Ability to establish and maintain relationships with patients, the care team, and sponsors.

Responsibilities

• Coordinate and participate in clinical research studies conducted by principal investigators.
• Collaborate with investigators to select appropriate studies to conduct.
• Complete study initiation procedures including regulatory submissions and source document creation.
• Maintain study files and communicate with sponsors and IRBs.
• Conduct protocol-defined patient visits, informed consent, education, lab collection, and dosing administration.
• Record vital signs and EKG collection as required by protocols.
• Coordinate with outside vendors for scheduling procedures.
• Report adverse events and complete sponsor data entry.
• Serve as primary contact for study patients and care team.

Skills

Detail-oriented

Communication

Regulatory knowledge

Medical terminology

Team collaboration

Problem solving

Education

Bachelor's degree in healthcare

Clinical research certification (CCRC/CRRP)

Job description

Nebraska Hematology-Oncology, PC. is seeking a Clinical Trials Coordinator to support multi-study oncology/hematology trials. You will manage regulatory processes, patient visits, and data entry under the supervision of the Clinical Trials Manager.

Responsibilities include initiating studies, coordinating with investigators, ensuring SOP compliance, and maintaining study materials and communications with sponsors and the care team.