Hybrid Clinical Research Coordinator I – Oncology Trials

Moffitt; Magnolia, Northern (AR, KY); Hybrid; USD 36.000 - 55.000; Teilzeit

Zusammenfassung

Moffitt Cancer Center is seeking a Clinical Research Coordinator I to support on-site clinical research activities at Magnolia Hospital. The CRC I coordinates patient care with medical staff and documents per regulatory guidelines under supervision.

The role involves screening, enrolling and following study subjects, with data and AE reporting, and liaison duties among investigators, regulatory staff and sponsors. Strong communication and organizational skills are essential.

Qualifikationen

• Bachelor’s degree in scientific, health-related or business admin; preferred.
• 1 year relevant clinical/health/science/business/research experience with a Bachelor’s degree.
• Associates degree with 2 years relevant experience if no bachelor’s.
• Oncology experience preferred.
• Knowledge of EMR (PowerChart) and trial management systems (OnCore).
• Experience with clinical trials and good clinical practices.

Aufgaben

• Coordinate on-site clinical research activities at Moffitt Cancer Center.
• Act as liaison between investigators, regulatory staff and sponsor.
• Screen, enroll and follow study subjects while ensuring protocol compliance.
• Manage data, source documentation and adverse event reporting.
• Perform administrative duties and maintain competent documentation.

Kenntnisse

Verbal communication

Written communication

Interpersonal skills

Time management

Teamwork

Ausbildung

Bachelor’s degree (preferred scientific/health/business)

Associates degree + 2 years experience

Tools

PowerChart

OnCore

EMR systems

Clinical trials knowledge

Jobbeschreibung

Moffitt Cancer Center is seeking a Clinical Research Coordinator I to support on-site clinical research activities at Magnolia Hospital. The CRC I coordinates patient care with medical staff and documents per regulatory guidelines under supervision.

The role involves screening, enrolling and following study subjects, with data and AE reporting, and liaison duties among investigators, regulatory staff and sponsors. Strong communication and organizational skills are essential.