Senior Cutaneous Clinical Trials Data Coordinator

CO2000 H. Lee Moffitt Cancer Center and Research Institute, Inc.; United States; Presencial; USD 35 000 - 53 000; Tempo integral

Resumo da oferta

The RDC III at CO2000 H. Lee Moffitt Cancer Center and Research Institute, Inc. is a senior data coordinator responsible for protocol-specific data extraction from medical records across multiple trials, ensuring alignment with good clinical practice and federal regulations.

The role handles high-volume, complex data, reviews source documents, and collaborates with investigators and study monitors to maintain data integrity and timely reporting.

Qualificações

• Education: High School Diploma/GED required
• Associate's degree with two years of research data management experience preferred
• Licensure/Certification: SOCRA/ACRP or equivalent
• Four years of experience with research data management required
• Clinical trial management systems and electronic medical record experience required

Responsabilidades

• The RDC III reviews and synthesizes information from medical records to extract trial data as specified by protocols
• Performs protocol-specific data requirements for multiple, diverse and complex research projects
• Maintains expertise to ensure data integrity and regulatory compliance for trials

Conhecimentos

Data management

EMR systems

Clinical trial systems

Communication skills

Formação académica

High School Diploma/GED

Associate degree preferred

Ferramentas

EMR systems

Clinical trial management software

Descrição da oferta de emprego

The RDC III at CO2000 H. Lee Moffitt Cancer Center and Research Institute, Inc. is a senior data coordinator responsible for protocol-specific data extraction from medical records across multiple trials, ensuring alignment with good clinical practice and federal regulations.

The role handles high-volume, complex data, reviews source documents, and collaborates with investigators and study monitors to maintain data integrity and timely reporting.