Hybrid Clinical Research Coordinator II - Cancer Trials

Moffitt Cancer Center; Wesley Chapel (NC); Híbrido; USD 60 000 - 75 000; Tempo integral

Resumo da oferta

The Clinical Research Coordinator II (CRC II) at Moffitt Cancer Center is a mid-level role within the CRC career path. You will support the Principal Investigator in clinical trials, implementing and coordinating research activities in accordance with standards and regulatory guidelines.

You will screen, enroll, and monitor study subjects, liaise between investigators, care providers, regulatory staff and sponsors, and perform core CRC duties for higher-volume, more complex studies.

Qualificações

• Bachelor’s degree with 2 years clinical trials coordination experience
• Associate’s degree with 4 years clinical trials coordination experience may be considered
• CCRP/CCRC certification preferred

Responsabilidades

• Support the Principal Investigator (PI) in clinical trials by implementing and coordinating research including administrative procedures.
• Coordinate patient care by collaborating with medical staff and documenting per regulatory guidelines.
• Act as liaison between investigators, care providers, regulatory staff and sponsors.
• Screen, enroll, and follow study subjects ensuring protocol compliance and close monitoring.
• Handle CRC core support and more complex duties with higher patient volume and evolving responsibilities

Conhecimentos

Clinical trials coordination

Team collaboration

Communication skills

Formação académica

Bachelor's degree

Associate degree with 4 years experience

CCRP/CCRC certification preferred

Descrição da oferta de emprego

The Clinical Research Coordinator II (CRC II) at Moffitt Cancer Center is a mid-level role within the CRC career path. You will support the Principal Investigator in clinical trials, implementing and coordinating research activities in accordance with standards and regulatory guidelines.

You will screen, enroll, and monitor study subjects, liaise between investigators, care providers, regulatory staff and sponsors, and perform core CRC duties for higher-volume, more complex studies.