Base: $31.83; bonus/equity: not specified; benefit...
On-site
Intermediate to advanced computer proficiency with excel and word
Ability to utilize electronic medical databases
Coordinate patient/study participant care
Yale Cancer Center is seeking a Data Coordinator 2 to support clinical trials through data management and patient coordination. The ideal candidate should possess strong technical skills, particularly in data handling and research coordination, and will work in a collaborative environment focused on cancer research and patient care
Job Summary
Yale Cancer Center is Connecticut's only cancer center designated as a Comprehensive Cancer Center by the National Cancer Institute (NCI).
The Clinical Research Assistant (CRA) will provide Yale Cancer Center/Clinical Trials Office with direct clinical and data management support related to the conduct of clinical trials.
Through the use of independent judgment and high-level decision- making, extract, record, and disseminate treatment-related information for regular reporting and monitoring by the research team and study sponsors.
Matching Summary
Match Score: 85
Yale Cancer Center is seeking a Data Coordinator 2 to support clinical trials through data management and patient coordination. The ideal candidate should possess strong technical skills, particularly in data handling and research coordination, and will work in a collaborative environment focused on cancer research and patient care.
Salary
Base: $31.83; Bonus/Equity: Not specified; Benefits: Not specified
Skills & Requirements
Must-have
Intermediate to advanced computer proficiency with Excel and Word
Ability to utilize electronic medical databases
Coordinate patient/study participant care
Independently and accurately abstract, create, and maintain research records
Source verify and enter data into sponsor databases
Impeccable interpersonal skills
Ability to work as a team and independently
Proven ability to multitask and maintain confidentiality
Organized and meticulous with details
Nice-to-have
Experience working with study sponsor personnel
Knowledge of Oracle software, Medidata Rave, EPIC and ONCORE
Knowledge of federal regulations for HIPAA and IRB
Experience working in a Clinical Trials setting
Oncology experience
Completion of Good Clinical Practice (GCP) training
Key Requirements
Two years of related work experience
Bachelor's degree in a related field
Equivalent combination of experience and education