Oncology Clinical Trials Coordinator

Nebraska Hematology Oncology PC; Lincoln (NE); Sur place; USD 55 000 - 75 000; Plein temps

Résumé du poste

Nebraska Hematology-Oncology, PC is seeking a Clinical Trials Coordinator to support a range of oncology/hematology studies. You will coordinate regulatory processes, participant visits, and cross-department activities under the supervision of the Clinical Trials Manager.

The role requires attention to detail, strong communication, and knowledge of SOPs, FDA regulations, and good documentation practices. Experience in clinical research is preferred, bachelor’s degree required.

Qualifications

• Detail-oriented with excellent communication skills.
• Experience interacting with patients, sponsors, and investigators.
• Knowledge of policies, regulations, and procedures for clinical research.

Responsabilités

• Coordinate and participate in clinical research studies led by principal investigators.
• Coordinate regulatory documents, initiation visits, and cross-department procedures.
• Conduct protocol-defined patient visits and informed consent processes.
• Record source data accurately and ensure proper billing of procedures.
• Maintain primary point of contact with study patients and care team.
• Assist in development and maintenance of SOPs related to research.
• Ensure compliance with FDA and regulatory guidelines.

Connaissances

Detail-oriented

Excellent communication

Interaction with patients and sponsors

Regulatory knowledge

Organizational skills

Safety awareness

Problem solving

Formation

Bachelor's degree in healthcare

Research experience

Clinical research certification (CCRC/CCRP)

Description du poste

Nebraska Hematology-Oncology, PC is seeking a Clinical Trials Coordinator to support a range of oncology/hematology studies. You will coordinate regulatory processes, participant visits, and cross-department activities under the supervision of the Clinical Trials Manager.

The role requires attention to detail, strong communication, and knowledge of SOPs, FDA regulations, and good documentation practices. Experience in clinical research is preferred, bachelor’s degree required.